Canonical Allele Identifier: CA2461408635

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551219G= , CM000685.2:g.139551219G=	GRCh38
NC_000023.10:g.138633378G= , CM000685.1:g.138633378G=	GRCh37
NC_000023.9:g.138461044G=	NCBI36
NG_007994.1:g.25484G= , LRG_556:g.25484G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.678G= MANE Select	ENSP00000218099.2:p.Arg226=
ENST00000643157.1:n.1345G=
ENST00000218099.6:c.678G=	ENSP00000218099.2:p.Arg226=
ENST00000394090.2:c.564G=	ENSP00000377650.2:p.Arg188=
NM_000133.3:c.678G= , LRG_556t1:c.678G=	NP_000124.1:p.Arg226=
NM_001313913.1:c.564G=	NP_001300842.1:p.Arg188=
XM_005262397.3:c.549G=	XP_005262454.1:p.Arg183=
XM_005262397.4:c.549G=	XP_005262454.1:p.Arg183=
NM_000133.4:c.678G= MANE Select	NP_000124.1:p.Arg226=
NM_001313913.2:c.564G=	NP_001300842.1:p.Arg188=