Canonical Allele Identifier: CA2461407821

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548488G= , CM000685.2:g.139548488G=	GRCh38
NC_000023.10:g.138630647G= , CM000685.1:g.138630647G=	GRCh37
NC_000023.9:g.138458313G=	NCBI36
NG_007994.1:g.22753G= , LRG_556:g.22753G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.517G= MANE Select	ENSP00000218099.2:p.Ala173=
ENST00000643157.1:n.1184G=
ENST00000218099.6:c.517G=	ENSP00000218099.2:p.Ala173=
ENST00000394090.2:c.403G=	ENSP00000377650.2:p.Ala135=
NM_000133.3:c.517G= , LRG_556t1:c.517G=	NP_000124.1:p.Ala173=
NM_001313913.1:c.403G=	NP_001300842.1:p.Ala135=
XM_005262397.3:c.392-2574G=	XP_005262454.1:n.392-2574G=
XM_005262397.4:c.392-2574G=	XP_005262454.1:n.392-2574G=
NM_000133.4:c.517G= MANE Select	NP_000124.1:p.Ala173=
NM_001313913.2:c.403G=	NP_001300842.1:p.Ala135=