Product Details

Primer Sequences

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Primer Chromosome Location

Chr.X: 110194079-110194584 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

AMMECR1

Entrez Gene ID

9949

Gene Name

Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1

Gene Aliases

AMMERC1

UniGene

Hs.656243

Gene Chromosome Location

Chr.X: 110194186-110440233 on Build GRCh38

Transcripts

NM_001025580.1 NM_001171689.1 NM_015365.2

SNP Detail

SNP ID	Chromosome Location
rs866328300	Chr.X: 110194407-110194407 on Build GRCh38
rs1014590684	Chr.X: 110194106-110194106 on Build GRCh38
rs748224214	Chr.X: 110194339-110194339 on Build GRCh38
rs975556788	Chr.X: 110194122-110194122 on Build GRCh38
rs757169959	Chr.X: 110194553-110194553 on Build GRCh38
rs759270588	Chr.X: 110194483-110194483 on Build GRCh38
rs765832527	Chr.X: 110194334-110194334 on Build GRCh38
rs12843653	Chr.X: 110194455-110194455 on Build GRCh38
rs978172758	Chr.X: 110194459-110194459 on Build GRCh38
rs905346934	Chr.X: 110194514-110194514 on Build GRCh38
rs183313414	Chr.X: 110194124-110194124 on Build GRCh38
rs914279107	Chr.X: 110194403-110194403 on Build GRCh38
rs924534173	Chr.X: 110194288-110194288 on Build GRCh38
rs139052898	Chr.X: 110194126-110194126 on Build GRCh38
rs374129100	Chr.X: 110194238-110194238 on Build GRCh38
rs953400206	Chr.X: 110194275-110194275 on Build GRCh38
rs948463179	Chr.X: 110194456-110194456 on Build GRCh38
rs755314596	Chr.X: 110194117-110194117 on Build GRCh38

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