Canonical Allele Identifier: CA2466845350

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957072C= , CM000685.2:g.154957072C=	GRCh38
NC_000023.10:g.154185347C= , CM000685.1:g.154185347C=	GRCh37
NC_000023.9:g.153838541C=	NCBI36
NG_011403.1:g.70652G=
NG_011403.2:g.70652G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1637G= MANE Select	ENSP00000353393.4:p.Arg546=
ENST00000647125.1:c.*1513G=	ENSP00000496062.1:n.*1513G=
ENST00000360256.8:c.1637G=	ENSP00000353393.4:p.Arg546=
NM_000132.3:c.1637G=	NP_000123.1:p.Arg546=
XM_011531126.1:c.1532G=	XP_011529428.1:p.Arg511=
NM_000132.4:c.1637G= MANE Select	NP_000123.1:p.Arg546=