Canonical Allele Identifier: CA2466849037

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969484G= , CM000685.2:g.154969484G=	GRCh38
NC_000023.10:g.154197759G= , CM000685.1:g.154197759G=	GRCh37
NC_000023.9:g.153850953G=	NCBI36
NG_011403.1:g.58240C=
NG_011403.2:g.58240C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.856C= MANE Select	ENSP00000353393.4:p.His286=
ENST00000647125.1:c.*732C=	ENSP00000496062.1:n.*732C=
ENST00000360256.8:c.856C=	ENSP00000353393.4:p.His286=
NM_000132.3:c.856C=	NP_000123.1:p.His286=
XM_011531126.1:c.751C=	XP_011529428.1:p.His251=
NM_000132.4:c.856C= MANE Select	NP_000123.1:p.His286=