Canonical Allele Identifier: CA2466856492

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154992938T= , CM000685.2:g.154992938T=	GRCh38
NC_000023.10:g.154221213T= , CM000685.1:g.154221213T=	GRCh37
NC_000023.9:g.153874407T=	NCBI36
NG_011403.1:g.34786A=
NG_011403.2:g.34786A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.599A= MANE Select	ENSP00000353393.4:p.Glu200=
ENST00000647125.1:c.*385A=	ENSP00000496062.1:n.*385A=
ENST00000360256.8:c.599A=	ENSP00000353393.4:p.Glu200=
ENST00000423959.5:c.494A=	ENSP00000409446.1:p.Glu165=
NM_000132.3:c.599A=	NP_000123.1:p.Glu200=
XM_011531126.1:c.494A=	XP_011529428.1:p.Glu165=
NM_000132.4:c.599A= MANE Select	NP_000123.1:p.Glu200=