Canonical Allele Identifier: CA2461412082

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561565C= , CM000685.2:g.139561565C=	GRCh38
NC_000023.10:g.138643724C= , CM000685.1:g.138643724C=	GRCh37
NC_000023.9:g.138471390C=	NCBI36
NG_007994.1:g.35830C= , LRG_556:g.35830C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000133.4:c.880C= MANE Select	NP_000124.1:p.Arg294=
ENST00000218099.7:c.880C= MANE Select	ENSP00000218099.2:p.Arg294=
NM_000133.3:c.880C= , LRG_556t1:c.880C=	NP_000124.1:p.Arg294=
NM_001313913.1:c.766C=	NP_001300842.1:p.Arg256=
NM_001313913.2:c.766C=	NP_001300842.1:p.Arg256=
ENST00000218099.6:c.880C=	ENSP00000218099.2:p.Arg294=
ENST00000394090.2:c.766C=	ENSP00000377650.2:p.Arg256=
ENST00000643157.1:n.1547C=
XM_005262397.3:c.751C=	XP_005262454.1:p.Arg251=
XM_005262397.4:c.751C=	XP_005262454.1:p.Arg251=