Canonical Allele Identifier: CA2466857753

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154996973C= , CM000685.2:g.154996973C=	GRCh38
NC_000023.10:g.154225248C= , CM000685.1:g.154225248C=	GRCh37
NC_000023.9:g.153878442C=	NCBI36
NG_011403.1:g.30751G=
NG_011403.2:g.30751G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.388G= MANE Select	ENSP00000353393.4:p.Gly130=
ENST00000647125.1:c.*174G=	ENSP00000496062.1:n.*174G=
ENST00000360256.8:c.388G=	ENSP00000353393.4:p.Gly130=
ENST00000423959.5:c.283G=	ENSP00000409446.1:p.Gly95=
ENST00000453950.1:c.370G=	ENSP00000389153.1:p.Gly124=
NM_000132.3:c.388G=	NP_000123.1:p.Gly130=
XM_011531126.1:c.283G=	XP_011529428.1:p.Gly95=
NM_000132.4:c.388G= MANE Select	NP_000123.1:p.Gly130=