Product Details

Primer Sequences
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Primer Chromosome Location
Chr.X: 139550859-139551118 on Build GRCh38
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
F9
Entrez Gene ID
2158
Gene Name
coagulation factor IX
Gene Aliases
F9 p22, FIX, HEMB, P19, PTC, THPH8
UniGene
Hs.522798
Gene Chromosome Location
Chr.X: 139530720-139563459 on Build GRCh38
Transcripts
NM_000133.3 NM_001313913.1 XM_005262397.4

SNP Detail

SNP ID Chromosome Location
rs893397544 Chr.X: 139550891-139550891 on Build GRCh38
rs950778820 Chr.X: 139551010-139551010 on Build GRCh38
rs371896578 Chr.X: 139551012-139551012 on Build GRCh38
rs978294440 Chr.X: 139550996-139550996 on Build GRCh38
rs774838331 Chr.X: 139550901-139550901 on Build GRCh38
rs587776736 Chr.X: 139551081-139551082 on Build GRCh38
rs995503262 Chr.X: 139550900-139550900 on Build GRCh38
rs765138918 Chr.X: 139551022-139551022 on Build GRCh38
rs962790137 Chr.X: 139550892-139550892 on Build GRCh38
rs924997267 Chr.X: 139551005-139551005 on Build GRCh38
rs1007778770 Chr.X: 139550899-139550899 on Build GRCh38
rs1026367643 Chr.X: 139550945-139550945 on Build GRCh38
rs775270217 Chr.X: 139551033-139551033 on Build GRCh38
rs992844428 Chr.X: 139550939-139550939 on Build GRCh38
rs762986355 Chr.X: 139551064-139551064 on Build GRCh38
rs998036360 Chr.X: 139550942-139550942 on Build GRCh38
rs759271387 Chr.X: 139550893-139550893 on Build GRCh38
rs387906477 Chr.X: 139551082-139551082 on Build GRCh38
rs967252255 Chr.X: 139550957-139550957 on Build GRCh38
rs760286256 Chr.X: 139550910-139550910 on Build GRCh38
rs959637546 Chr.X: 139550932-139550933 on Build GRCh38
rs901989842 Chr.X: 139550929-139550929 on Build GRCh38

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