Canonical Allele Identifier: CA2466835769

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154928689C= , CM000685.2:g.154928689C=	GRCh38
NC_000023.10:g.154156964C= , CM000685.1:g.154156964C=	GRCh37
NC_000023.9:g.153810158C=	NCBI36
NG_011403.1:g.99035G=
NG_011403.2:g.99035G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5101G= MANE Select	ENSP00000353393.4:p.Glu1701=
ENST00000360256.8:c.5101G=	ENSP00000353393.4:p.Glu1701=
NM_000132.3:c.5101G=	NP_000123.1:p.Glu1701=
XM_011531126.1:c.4996G=	XP_011529428.1:p.Glu1666=
NM_000132.4:c.5101G= MANE Select	NP_000123.1:p.Glu1701=