Canonical Allele Identifier: CA2466835767

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154928682T= , CM000685.2:g.154928682T=	GRCh38
NC_000023.10:g.154156957T= , CM000685.1:g.154156957T=	GRCh37
NC_000023.9:g.153810151T=	NCBI36
NG_011403.1:g.99042A=
NG_011403.2:g.99042A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.5108A= MANE Select	ENSP00000353393.4:p.Glu1703=
ENST00000360256.8:c.5108A=	ENSP00000353393.4:p.Glu1703=
NM_000132.3:c.5108A=	NP_000123.1:p.Glu1703=
XM_011531126.1:c.5003A=	XP_011529428.1:p.Glu1668=
NM_000132.4:c.5108A= MANE Select	NP_000123.1:p.Glu1703=