Canonical Allele Identifier: CA255439
Gene: F9 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 10649
ClinVar RCV Id: RCV000011395
dbSNP Id: rs137852276

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561917G>T , CM000685.2:g.139561917G>T GRCh38
NC_000023.10:g.138644076G>T , CM000685.1:g.138644076G>T GRCh37
NC_000023.9:g.138471742G>T NCBI36
NG_007994.1:g.36182G>T , LRG_556:g.36182G>T

Transcript Alleles

HGVS Amino-acid change
NM_000133.3:c.1232G>T , LRG_556t1:c.1232G>T NP_000124.1:p.Ser411Ile
NM_001313913.1:c.1118G>T VV NP_001300842.1:p.Ser373Ile
XM_005262397.3:c.1103G>T XP_005262454.1:p.Ser368Ile
XM_005262397.4:c.1103G>T XP_005262454.1:p.Ser368Ile
ENST00000218099.6:c.1232G>T ENSP00000218099.2:p.Ser411Ile
ENST00000394090.2:n.1118G>T ENSP00000377650.2:p.Ser373Ile