Canonical Allele Identifier: CA255344
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10587
dbSNP Id: rs137852248

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561565C>T , CM000685.2:g.139561565C>T GRCh38
NC_000023.10:g.138643724C>T , CM000685.1:g.138643724C>T GRCh37
NC_000023.9:g.138471390C>T NCBI36
NG_007994.1:g.35830C>T , LRG_556:g.35830C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.880C>T MANE Select ENSP00000218099.2:p.Arg294Ter
ENST00000643157.1:n.1547C>T
ENST00000218099.6:c.880C>T ENSP00000218099.2:p.Arg294Ter
ENST00000394090.2:n.766C>T ENSP00000377650.2:p.Arg256Ter
NM_000133.3:c.880C>T , LRG_556t1:c.880C>T NP_000124.1:p.Arg294Ter
NM_001313913.1:c.766C>T NP_001300842.1:p.Arg256Ter
XM_005262397.3:c.751C>T XP_005262454.1:p.Arg251Ter
XM_005262397.4:c.751C>T XP_005262454.1:p.Arg251Ter
NM_000133.4:c.880C>T MANE Select NP_000124.1:p.Arg294Ter
NM_001313913.2:c.766C>T NP_001300842.1:p.Arg256Ter