Canonical Allele Identifier: CA2461407804

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548443A= , CM000685.2:g.139548443A=	GRCh38
NC_000023.10:g.138630602A= , CM000685.1:g.138630602A=	GRCh37
NC_000023.9:g.138458268A=	NCBI36
NG_007994.1:g.22708A= , LRG_556:g.22708A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.472A= MANE Select	ENSP00000218099.2:p.Thr158=
ENST00000643157.1:n.1139A=
ENST00000218099.6:c.472A=	ENSP00000218099.2:p.Thr158=
ENST00000394090.2:c.358A=	ENSP00000377650.2:p.Thr120=
NM_000133.3:c.472A= , LRG_556t1:c.472A=	NP_000124.1:p.Thr158=
NM_001313913.1:c.358A=	NP_001300842.1:p.Thr120=
XM_005262397.3:c.392-2619A=	XP_005262454.1:n.392-2619A=
XM_005262397.4:c.392-2619A=	XP_005262454.1:n.392-2619A=
NM_000133.4:c.472A= MANE Select	NP_000124.1:p.Thr158=
NM_001313913.2:c.358A=	NP_001300842.1:p.Thr120=