Canonical Allele Identifier: CA2466857798

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997077A= , CM000685.2:g.154997077A=	GRCh38
NC_000023.10:g.154225352A= , CM000685.1:g.154225352A=	GRCh37
NC_000023.9:g.153878546A=	NCBI36
NG_011403.1:g.30647T=
NG_011403.2:g.30647T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.284T= MANE Select	ENSP00000353393.4:p.Ile95=
ENST00000647125.1:c.*70T=	ENSP00000496062.1:n.*70T=
ENST00000360256.8:c.284T=	ENSP00000353393.4:p.Ile95=
ENST00000423959.5:c.179T=	ENSP00000409446.1:p.Ile60=
ENST00000453950.1:c.266T=	ENSP00000389153.1:p.Ile89=
NM_000132.3:c.284T=	NP_000123.1:p.Ile95=
XM_011531126.1:c.179T=	XP_011529428.1:p.Ile60=
NM_000132.4:c.284T= MANE Select	NP_000123.1:p.Ile95=