Canonical Allele Identifier: CA2461412073

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561544A= , CM000685.2:g.139561544A=	GRCh38
NC_000023.10:g.138643703A= , CM000685.1:g.138643703A=	GRCh37
NC_000023.9:g.138471369A=	NCBI36
NG_007994.1:g.35809A= , LRG_556:g.35809A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.859A= MANE Select	ENSP00000218099.2:p.Thr287=
ENST00000643157.1:n.1526A=
ENST00000218099.6:c.859A=	ENSP00000218099.2:p.Thr287=
ENST00000394090.2:c.745A=	ENSP00000377650.2:p.Thr249=
NM_000133.3:c.859A= , LRG_556t1:c.859A=	NP_000124.1:p.Thr287=
NM_001313913.1:c.745A=	NP_001300842.1:p.Thr249=
XM_005262397.3:c.730A=	XP_005262454.1:p.Thr244=
XM_005262397.4:c.730A=	XP_005262454.1:p.Thr244=
NM_000133.4:c.859A= MANE Select	NP_000124.1:p.Thr287=
NM_001313913.2:c.745A=	NP_001300842.1:p.Thr249=