Canonical Allele Identifier: CA2466857784

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997048T= , CM000685.2:g.154997048T=	GRCh38
NC_000023.10:g.154225323T= , CM000685.1:g.154225323T=	GRCh37
NC_000023.9:g.153878517T=	NCBI36
NG_011403.1:g.30676A=
NG_011403.2:g.30676A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.313A= MANE Select	ENSP00000353393.4:p.Ile105=
ENST00000647125.1:c.*99A=	ENSP00000496062.1:n.*99A=
ENST00000360256.8:c.313A=	ENSP00000353393.4:p.Ile105=
ENST00000423959.5:c.208A=	ENSP00000409446.1:p.Ile70=
ENST00000453950.1:c.295A=	ENSP00000389153.1:p.Ile99=
NM_000132.3:c.313A=	NP_000123.1:p.Ile105=
XM_011531126.1:c.208A=	XP_011529428.1:p.Ile70=
NM_000132.4:c.313A= MANE Select	NP_000123.1:p.Ile105=