Product Details

Primer Sequences

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Primer Chromosome Location

Chr.13: 77902977-77903238 on Build GRCh38 View in UCSC browser

Format

Each primer will be delivered in a single tube, dried-down

Quick Reference Guide

Primer Designer^™ Tool Quick Reference

Ampliseq ID's

Gene Details

Gene Symbol

EDNRB

Entrez Gene ID

1910

Gene Name

endothelin receptor type B

Gene Aliases

ABCDS, ET-B, ET-BR, ETB, ETB1, ETBR, ETRB, HSCR, HSCR2, WS4A

UniGene

Hs.732046

Gene Chromosome Location

Chr.13: 77895481-77975529 on Build GRCh38

Transcripts

NM_000115.3 NM_001122659.2 NM_001201397.1 NM_003991.3 NR_103853.1

Gene Symbol

EDNRB-AS1

Entrez Gene ID

100505518

Gene Name

EDNRB antisense RNA 1

Gene Aliases

-

UniGene

Hs.742215

Gene Chromosome Location

Chr.13: 77818937-77908442 on Build GRCh38

Transcripts

NM_000115.3 NM_001122659.2 NM_001201397.1 NM_003991.3 NR_103853.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
432583	c.787A>G	p.T263A	Chr.13: 77903170-77903170 on Build GRCh38
4680212	c.777C>T	p.P259P	Chr.13: 77903180-77903180 on Build GRCh38
6139576	c.727A>G	p.I243V	Chr.13: 77903230-77903230 on Build GRCh38
1950562	c.1027C>T	p.R343*	Chr.13: 77903200-77903200 on Build GRCh38
4457371	c.1042C>T	p.H348Y	Chr.13: 77903185-77903185 on Build GRCh38
1950557	c.778G>A	p.V260I	Chr.13: 77903179-77903179 on Build GRCh38
1300317	c.1029A>G	p.R343R	Chr.13: 77903198-77903198 on Build GRCh38
1250941	c.1051C>A	p.Q351K	Chr.13: 77903176-77903176 on Build GRCh38
5909327	c.1046C>T	p.P349L	Chr.13: 77903181-77903181 on Build GRCh38
4680214	c.732G>A	p.T244T	Chr.13: 77903225-77903225 on Build GRCh38
5684525	c.765C>A	p.C255*	Chr.13: 77903192-77903192 on Build GRCh38
5742626	c.731C>T	p.T244M	Chr.13: 77903226-77903226 on Build GRCh38
1950563	c.757C>T	p.R253*	Chr.13: 77903200-77903200 on Build GRCh38
4048574	c.782A>C	p.Q261P	Chr.13: 77903175-77903175 on Build GRCh38
3704714	c.801+8T>C	p.?	Chr.13: 77903148-77903148 on Build GRCh38
1152669	c.1061C>T	p.A354V	Chr.13: 77903166-77903166 on Build GRCh38
4680210	c.1047C>T	p.P349P	Chr.13: 77903180-77903180 on Build GRCh38
1477322	c.1057A>G	p.T353A	Chr.13: 77903170-77903170 on Build GRCh38
4048573	c.1052A>C	p.Q351P	Chr.13: 77903175-77903175 on Build GRCh38
4680215	c.732G>A	p.T244T	Chr.13: 77903225-77903225 on Build GRCh38
5909328	c.776C>T	p.P259L	Chr.13: 77903181-77903181 on Build GRCh38
3793392	c.1058C>T	p.T353I	Chr.13: 77903169-77903169 on Build GRCh38
1950556	c.1048G>A	p.V350I	Chr.13: 77903179-77903179 on Build GRCh38
948731	c.791C>T	p.A264V	Chr.13: 77903166-77903166 on Build GRCh38
3704713	c.801+8T>C	p.?	Chr.13: 77903148-77903148 on Build GRCh38
6563547	c.1058C>A	p.T353K	Chr.13: 77903169-77903169 on Build GRCh38
4680211	c.777C>T	p.P259P	Chr.13: 77903180-77903180 on Build GRCh38
4048575	c.782A>C	p.Q261P	Chr.13: 77903175-77903175 on Build GRCh38
6563548	c.788C>A	p.T263K	Chr.13: 77903169-77903169 on Build GRCh38
1950558	c.778G>A	p.V260I	Chr.13: 77903179-77903179 on Build GRCh38
4814525	c.787A>G	p.T263A	Chr.13: 77903170-77903170 on Build GRCh38
3704712	c.1071+8T>C	p.?	Chr.13: 77903148-77903148 on Build GRCh38
5909329	c.776C>T	p.P259L	Chr.13: 77903181-77903181 on Build GRCh38
3793394	c.788C>T	p.T263I	Chr.13: 77903169-77903169 on Build GRCh38
4680213	c.1002G>A	p.T334T	Chr.13: 77903225-77903225 on Build GRCh38
4457373	c.772C>T	p.H258Y	Chr.13: 77903185-77903185 on Build GRCh38
4812479	c.759A>G	p.R253R	Chr.13: 77903198-77903198 on Build GRCh38
5684524	c.1035C>A	p.C345*	Chr.13: 77903192-77903192 on Build GRCh38
6139575	c.727A>G	p.I243V	Chr.13: 77903230-77903230 on Build GRCh38
5742627	c.731C>T	p.T244M	Chr.13: 77903226-77903226 on Build GRCh38
5742625	c.1001C>T	p.T334M	Chr.13: 77903226-77903226 on Build GRCh38
6563549	c.788C>A	p.T263K	Chr.13: 77903169-77903169 on Build GRCh38
280719	c.757C>T	p.R253*	Chr.13: 77903200-77903200 on Build GRCh38
1300318	c.759A>G	p.R253R	Chr.13: 77903198-77903198 on Build GRCh38
5684526	c.765C>A	p.C255*	Chr.13: 77903192-77903192 on Build GRCh38
4457372	c.772C>T	p.H258Y	Chr.13: 77903185-77903185 on Build GRCh38
3793393	c.788C>T	p.T263I	Chr.13: 77903169-77903169 on Build GRCh38
1250942	c.781C>A	p.Q261K	Chr.13: 77903176-77903176 on Build GRCh38
6139574	c.997A>G	p.I333V	Chr.13: 77903230-77903230 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs754040927	Chr.13: 77903202-77903202 on Build GRCh38
rs140514830	Chr.13: 77903199-77903199 on Build GRCh38
rs104894390	Chr.13: 77903200-77903200 on Build GRCh38
rs375637651	Chr.13: 77903180-77903180 on Build GRCh38
rs879113182	Chr.13: 77903184-77903184 on Build GRCh38
rs77132068	Chr.13: 77903179-77903179 on Build GRCh38
rs377488350	Chr.13: 77903127-77903127 on Build GRCh38
rs977380746	Chr.13: 77903204-77903204 on Build GRCh38
rs370977355	Chr.13: 77903136-77903136 on Build GRCh38
rs899618795	Chr.13: 77903025-77903025 on Build GRCh38
rs750477425	Chr.13: 77903197-77903197 on Build GRCh38
rs1033388767	Chr.13: 77903138-77903138 on Build GRCh38
rs200431358	Chr.13: 77903182-77903182 on Build GRCh38
rs530578139	Chr.13: 77903094-77903094 on Build GRCh38
rs768394514	Chr.13: 77903114-77903114 on Build GRCh38
rs932392755	Chr.13: 77903066-77903067 on Build GRCh38
rs749117704	Chr.13: 77903113-77903113 on Build GRCh38
rs201072847	Chr.13: 77903174-77903174 on Build GRCh38
rs772585011	Chr.13: 77903131-77903131 on Build GRCh38
rs368940609	Chr.13: 77903185-77903185 on Build GRCh38
rs570185768	Chr.13: 77903147-77903147 on Build GRCh38
rs748047611	Chr.13: 77903125-77903125 on Build GRCh38
rs778871426	Chr.13: 77903124-77903124 on Build GRCh38
rs3027107	Chr.13: 77903008-77903008 on Build GRCh38
rs371057149	Chr.13: 77903196-77903196 on Build GRCh38
rs147868826	Chr.13: 77903108-77903108 on Build GRCh38
rs890940624	Chr.13: 77903089-77903089 on Build GRCh38
rs1009840735	Chr.13: 77903060-77903060 on Build GRCh38
rs892381661	Chr.13: 77903046-77903046 on Build GRCh38
rs1046252347	Chr.13: 77903100-77903100 on Build GRCh38
rs752147666	Chr.13: 77903183-77903183 on Build GRCh38
rs1051385989	Chr.13: 77903073-77903073 on Build GRCh38

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