Canonical Allele Identifier: CA2461412077

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561556G= , CM000685.2:g.139561556G=	GRCh38
NC_000023.10:g.138643715G= , CM000685.1:g.138643715G=	GRCh37
NC_000023.9:g.138471381G=	NCBI36
NG_007994.1:g.35821G= , LRG_556:g.35821G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.871G= MANE Select	ENSP00000218099.2:p.Glu291=
ENST00000643157.1:n.1538G=
ENST00000218099.6:c.871G=	ENSP00000218099.2:p.Glu291=
ENST00000394090.2:c.757G=	ENSP00000377650.2:p.Glu253=
NM_000133.3:c.871G= , LRG_556t1:c.871G=	NP_000124.1:p.Glu291=
NM_001313913.1:c.757G=	NP_001300842.1:p.Glu253=
XM_005262397.3:c.742G=	XP_005262454.1:p.Glu248=
XM_005262397.4:c.742G=	XP_005262454.1:p.Glu248=
NM_000133.4:c.871G= MANE Select	NP_000124.1:p.Glu291=
NM_001313913.2:c.757G=	NP_001300842.1:p.Glu253=