Canonical Allele Identifier: CA2466857800

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997080G= , CM000685.2:g.154997080G=	GRCh38
NC_000023.10:g.154225355G= , CM000685.1:g.154225355G=	GRCh37
NC_000023.9:g.153878549G=	NCBI36
NG_011403.1:g.30644C=
NG_011403.2:g.30644C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.281C= MANE Select	ENSP00000353393.4:p.Thr94=
ENST00000647125.1:c.*67C=	ENSP00000496062.1:n.*67C=
ENST00000360256.8:c.281C=	ENSP00000353393.4:p.Thr94=
ENST00000423959.5:c.176C=	ENSP00000409446.1:p.Thr59=
ENST00000453950.1:c.263C=	ENSP00000389153.1:p.Thr88=
NM_000132.3:c.281C=	NP_000123.1:p.Thr94=
XM_011531126.1:c.176C=	XP_011529428.1:p.Thr59=
NM_000132.4:c.281C= MANE Select	NP_000123.1:p.Thr94=