Canonical Allele Identifier: CA2461408649

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551251A= , CM000685.2:g.139551251A=	GRCh38
NC_000023.10:g.138633410A= , CM000685.1:g.138633410A=	GRCh37
NC_000023.9:g.138461076A=	NCBI36
NG_007994.1:g.25516A= , LRG_556:g.25516A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.710A= MANE Select	ENSP00000218099.2:p.Gln237=
ENST00000643157.1:n.1377A=
ENST00000218099.6:c.710A=	ENSP00000218099.2:p.Gln237=
ENST00000394090.2:c.596A=	ENSP00000377650.2:p.Gln199=
NM_000133.3:c.710A= , LRG_556t1:c.710A=	NP_000124.1:p.Gln237=
NM_001313913.1:c.596A=	NP_001300842.1:p.Gln199=
XM_005262397.3:c.581A=	XP_005262454.1:p.Gln194=
XM_005262397.4:c.581A=	XP_005262454.1:p.Gln194=
NM_000133.4:c.710A= MANE Select	NP_000124.1:p.Gln237=
NM_001313913.2:c.596A=	NP_001300842.1:p.Gln199=