Canonical Allele Identifier: CA2461407775

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548370A= , CM000685.2:g.139548370A=	GRCh38
NC_000023.10:g.138630529A= , CM000685.1:g.138630529A=	GRCh37
NC_000023.9:g.138458195A=	NCBI36
NG_007994.1:g.22635A= , LRG_556:g.22635A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.399A= MANE Select	ENSP00000218099.2:p.Thr133=
ENST00000643157.1:n.1066A=
ENST00000218099.6:c.399A=	ENSP00000218099.2:p.Thr133=
ENST00000394090.2:c.285A=	ENSP00000377650.2:p.Thr95=
ENST00000479617.2:n.352A=
NM_000133.3:c.399A= , LRG_556t1:c.399A=	NP_000124.1:p.Thr133=
NM_001313913.1:c.285A=	NP_001300842.1:p.Thr95=
XM_005262397.3:c.392-2692A=	XP_005262454.1:n.392-2692A=
XM_005262397.4:c.392-2692A=	XP_005262454.1:n.392-2692A=
NM_000133.4:c.399A= MANE Select	NP_000124.1:p.Thr133=
NM_001313913.2:c.285A=	NP_001300842.1:p.Thr95=