Canonical Allele Identifier: CA2461411810

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560755T= , CM000685.2:g.139560755T=	GRCh38
NC_000023.10:g.138642914T= , CM000685.1:g.138642914T=	GRCh37
NC_000023.9:g.138470580T=	NCBI36
NG_007994.1:g.35020T= , LRG_556:g.35020T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.738T= MANE Select	ENSP00000218099.2:p.Gly246=
ENST00000643157.1:n.1405T=
ENST00000218099.6:c.738T=	ENSP00000218099.2:p.Gly246=
ENST00000394090.2:c.624T=	ENSP00000377650.2:p.Gly208=
NM_000133.3:c.738T= , LRG_556t1:c.738T=	NP_000124.1:p.Gly246=
NM_001313913.1:c.624T=	NP_001300842.1:p.Gly208=
XM_005262397.3:c.609T=	XP_005262454.1:p.Gly203=
XM_005262397.4:c.609T=	XP_005262454.1:p.Gly203=
NM_000133.4:c.738T= MANE Select	NP_000124.1:p.Gly246=
NM_001313913.2:c.624T=	NP_001300842.1:p.Gly208=