Canonical Allele Identifier: CA2466857785

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997049G= , CM000685.2:g.154997049G=	GRCh38
NC_000023.10:g.154225324G= , CM000685.1:g.154225324G=	GRCh37
NC_000023.9:g.153878518G=	NCBI36
NG_011403.1:g.30675C=
NG_011403.2:g.30675C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.312C= MANE Select	ENSP00000353393.4:p.Val104=
ENST00000647125.1:c.*98C=	ENSP00000496062.1:n.*98C=
ENST00000360256.8:c.312C=	ENSP00000353393.4:p.Val104=
ENST00000423959.5:c.207C=	ENSP00000409446.1:p.Val69=
ENST00000453950.1:c.294C=	ENSP00000389153.1:p.Val98=
NM_000132.3:c.312C=	NP_000123.1:p.Val104=
XM_011531126.1:c.207C=	XP_011529428.1:p.Val69=
NM_000132.4:c.312C= MANE Select	NP_000123.1:p.Val104=