Canonical Allele Identifier: CA255418
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10624
ClinVar RCV Id: RCV000011370
dbSNP Id: rs137852267

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562009G>A , CM000685.2:g.139562009G>A GRCh38
NC_000023.10:g.138644168G>A , CM000685.1:g.138644168G>A GRCh37
NC_000023.9:g.138471834G>A NCBI36
NG_007994.1:g.36274G>A , LRG_556:g.36274G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1324G>A MANE Select ENSP00000218099.2:p.Gly442Arg
ENST00000643157.1:n.1723+268G>A
ENST00000218099.6:c.1324G>A ENSP00000218099.2:p.Gly442Arg
ENST00000394090.2:n.1210G>A ENSP00000377650.2:p.Gly404Arg
NM_000133.3:c.1324G>A , LRG_556t1:c.1324G>A NP_000124.1:p.Gly442Arg
NM_001313913.1:c.1210G>A NP_001300842.1:p.Gly404Arg
XM_005262397.3:c.1195G>A XP_005262454.1:p.Gly399Arg
XM_005262397.4:c.1195G>A XP_005262454.1:p.Gly399Arg
NM_000133.4:c.1324G>A MANE Select NP_000124.1:p.Gly442Arg
NM_001313913.2:c.1210G>A NP_001300842.1:p.Gly404Arg