Canonical Allele Identifier: CA2461412117

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561649G= , CM000685.2:g.139561649G=	GRCh38
NC_000023.10:g.138643808G= , CM000685.1:g.138643808G=	GRCh37
NC_000023.9:g.138471474G=	NCBI36
NG_007994.1:g.35914G= , LRG_556:g.35914G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.964G= MANE Select	ENSP00000218099.2:p.Asp322=
ENST00000643157.1:n.1631G=
ENST00000218099.6:c.964G=	ENSP00000218099.2:p.Asp322=
ENST00000394090.2:c.850G=	ENSP00000377650.2:p.Asp284=
NM_000133.3:c.964G= , LRG_556t1:c.964G=	NP_000124.1:p.Asp322=
NM_001313913.1:c.850G=	NP_001300842.1:p.Asp284=
XM_005262397.3:c.835G=	XP_005262454.1:p.Asp279=
XM_005262397.4:c.835G=	XP_005262454.1:p.Asp279=
NM_000133.4:c.964G= MANE Select	NP_000124.1:p.Asp322=
NM_001313913.2:c.850G=	NP_001300842.1:p.Asp284=