Canonical Allele Identifier: CA2461412134

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561694G= , CM000685.2:g.139561694G=	GRCh38
NC_000023.10:g.138643853G= , CM000685.1:g.138643853G=	GRCh37
NC_000023.9:g.138471519G=	NCBI36
NG_007994.1:g.35959G= , LRG_556:g.35959G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1009G= MANE Select	ENSP00000218099.2:p.Ala337=
ENST00000643157.1:n.1676G=
ENST00000218099.6:c.1009G=	ENSP00000218099.2:p.Ala337=
ENST00000394090.2:c.895G=	ENSP00000377650.2:p.Ala299=
NM_000133.3:c.1009G= , LRG_556t1:c.1009G=	NP_000124.1:p.Ala337=
NM_001313913.1:c.895G=	NP_001300842.1:p.Ala299=
XM_005262397.3:c.880G=	XP_005262454.1:p.Ala294=
XM_005262397.4:c.880G=	XP_005262454.1:p.Ala294=
NM_000133.4:c.1009G= MANE Select	NP_000124.1:p.Ala337=
NM_001313913.2:c.895G=	NP_001300842.1:p.Ala299=