Canonical Allele Identifier: CA2466845366

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957132T= , CM000685.2:g.154957132T=	GRCh38
NC_000023.10:g.154185407T= , CM000685.1:g.154185407T=	GRCh37
NC_000023.9:g.153838601T=	NCBI36
NG_011403.1:g.70592A=
NG_011403.2:g.70592A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1577A= MANE Select	ENSP00000353393.4:p.Glu526=
ENST00000647125.1:c.*1453A=	ENSP00000496062.1:n.*1453A=
ENST00000360256.8:c.1577A=	ENSP00000353393.4:p.Glu526=
NM_000132.3:c.1577A=	NP_000123.1:p.Glu526=
XM_011531126.1:c.1472A=	XP_011529428.1:p.Glu491=
NM_000132.4:c.1577A= MANE Select	NP_000123.1:p.Glu526=