Canonical Allele Identifier: CA2461412142

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561716T= , CM000685.2:g.139561716T=	GRCh38
NC_000023.10:g.138643875T= , CM000685.1:g.138643875T=	GRCh37
NC_000023.9:g.138471541T=	NCBI36
NG_007994.1:g.35981T= , LRG_556:g.35981T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1031T= MANE Select	ENSP00000218099.2:p.Ile344=
ENST00000643157.1:n.1698T=
ENST00000218099.6:c.1031T=	ENSP00000218099.2:p.Ile344=
ENST00000394090.2:c.917T=	ENSP00000377650.2:p.Ile306=
NM_000133.3:c.1031T= , LRG_556t1:c.1031T=	NP_000124.1:p.Ile344=
NM_001313913.1:c.917T=	NP_001300842.1:p.Ile306=
XM_005262397.3:c.902T=	XP_005262454.1:p.Ile301=
XM_005262397.4:c.902T=	XP_005262454.1:p.Ile301=
NM_000133.4:c.1031T= MANE Select	NP_000124.1:p.Ile344=
NM_001313913.2:c.917T=	NP_001300842.1:p.Ile306=