Canonical Allele Identifier: CA2466857793

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997067C= , CM000685.2:g.154997067C=	GRCh38
NC_000023.10:g.154225342C= , CM000685.1:g.154225342C=	GRCh37
NC_000023.9:g.153878536C=	NCBI36
NG_011403.1:g.30657G=
NG_011403.2:g.30657G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.294G= MANE Select	ENSP00000353393.4:p.Glu98=
ENST00000647125.1:c.*80G=	ENSP00000496062.1:n.*80G=
ENST00000360256.8:c.294G=	ENSP00000353393.4:p.Glu98=
ENST00000423959.5:c.189G=	ENSP00000409446.1:p.Glu63=
ENST00000453950.1:c.276G=	ENSP00000389153.1:p.Glu92=
NM_000132.3:c.294G=	NP_000123.1:p.Glu98=
XM_011531126.1:c.189G=	XP_011529428.1:p.Glu63=
NM_000132.4:c.294G= MANE Select	NP_000123.1:p.Glu98=