Canonical Allele Identifier: CA2466848105

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154966479A= , CM000685.2:g.154966479A=	GRCh38
NC_000023.10:g.154194754A= , CM000685.1:g.154194754A=	GRCh37
NC_000023.9:g.153847948A=	NCBI36
NG_011403.1:g.61245T=
NG_011403.2:g.61245T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1218T= MANE Select	ENSP00000353393.4:p.Ala406=
ENST00000647125.1:c.*1094T=	ENSP00000496062.1:n.*1094T=
ENST00000360256.8:c.1218T=	ENSP00000353393.4:p.Ala406=
ENST00000483822.2:n.38T=
NM_000132.3:c.1218T=	NP_000123.1:p.Ala406=
XM_011531126.1:c.1113T=	XP_011529428.1:p.Ala371=
NM_000132.4:c.1218T= MANE Select	NP_000123.1:p.Ala406=