Canonical Allele Identifier: CA2461412088

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561578G= , CM000685.2:g.139561578G=	GRCh38
NC_000023.10:g.138643737G= , CM000685.1:g.138643737G=	GRCh37
NC_000023.9:g.138471403G=	NCBI36
NG_007994.1:g.35843G= , LRG_556:g.35843G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.893G= MANE Select	ENSP00000218099.2:p.Arg298=
ENST00000643157.1:n.1560G=
ENST00000218099.6:c.893G=	ENSP00000218099.2:p.Arg298=
ENST00000394090.2:c.779G=	ENSP00000377650.2:p.Arg260=
NM_000133.3:c.893G= , LRG_556t1:c.893G=	NP_000124.1:p.Arg298=
NM_001313913.1:c.779G=	NP_001300842.1:p.Arg260=
XM_005262397.3:c.764G=	XP_005262454.1:p.Arg255=
XM_005262397.4:c.764G=	XP_005262454.1:p.Arg255=
NM_000133.4:c.893G= MANE Select	NP_000124.1:p.Arg298=
NM_001313913.2:c.779G=	NP_001300842.1:p.Arg260=