Canonical Allele Identifier: CA1139532183

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903942C= , CM000685.2:g.154903942C=	GRCh38
NC_000023.10:g.154132217C= , CM000685.1:g.154132217C=	GRCh37
NC_000023.9:g.153785411C=	NCBI36
NG_011403.1:g.123782G=
NG_011403.2:g.123782G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5962G= MANE Select	ENSP00000353393.4:p.Glu1988=
ENST00000360256.8:c.5962G=	ENSP00000353393.4:p.Glu1988=
NM_000132.3:c.5962G=	NP_000123.1:p.Glu1988=
XM_011531126.1:c.5857G=	XP_011529428.1:p.Glu1953=
NM_000132.4:c.5962G= MANE Select	NP_000123.1:p.Glu1988=