Canonical Allele Identifier: CA10529870
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 368002
dbSNP Id: rs112057482

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561780A>G , CM000685.2:g.139561780A>G GRCh38
NC_000023.10:g.138643939A>G , CM000685.1:g.138643939A>G GRCh37
NC_000023.9:g.138471605A>G NCBI36
NG_007994.1:g.36045A>G , LRG_556:g.36045A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.1095A>G MANE Select ENSP00000218099.2:p.Ser365=
ENST00000643157.1:n.1723+39A>G
ENST00000218099.6:c.1095A>G ENSP00000218099.2:p.Ser365=
ENST00000394090.2:c.981A>G ENSP00000377650.2:p.Ser327=
NM_000133.3:c.1095A>G , LRG_556t1:c.1095A>G NP_000124.1:p.Ser365=
NM_001313913.1:c.981A>G NP_001300842.1:p.Ser327=
XM_005262397.3:c.966A>G XP_005262454.1:p.Ser322=
XM_005262397.4:c.966A>G XP_005262454.1:p.Ser322=
NM_000133.4:c.1095A>G MANE Select NP_000124.1:p.Ser365=
NM_001313913.2:c.981A>G NP_001300842.1:p.Ser327=