Canonical Allele Identifier: CA2461408608

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551125T= , CM000685.2:g.139551125T=	GRCh38
NC_000023.10:g.138633284T= , CM000685.1:g.138633284T=	GRCh37
NC_000023.9:g.138460950T=	NCBI36
NG_007994.1:g.25390T= , LRG_556:g.25390T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.584T= MANE Select	ENSP00000218099.2:p.Val195=
ENST00000643157.1:n.1251T=
ENST00000218099.6:c.584T=	ENSP00000218099.2:p.Val195=
ENST00000394090.2:c.470T=	ENSP00000377650.2:p.Val157=
NM_000133.3:c.584T= , LRG_556t1:c.584T=	NP_000124.1:p.Val195=
NM_001313913.1:c.470T=	NP_001300842.1:p.Val157=
XM_005262397.3:c.455T=	XP_005262454.1:p.Val152=
XM_005262397.4:c.455T=	XP_005262454.1:p.Val152=
NM_000133.4:c.584T= MANE Select	NP_000124.1:p.Val195=
NM_001313913.2:c.470T=	NP_001300842.1:p.Val157=