Canonical Allele Identifier: CA2466865507

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022706A= , CM000685.2:g.155022706A=	GRCh38
NC_000023.10:g.154250981A= , CM000685.1:g.154250981A=	GRCh37
NC_000023.9:g.153904175A=	NCBI36
NG_011403.1:g.5018T=
NG_011403.2:g.5018T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-154T= MANE Select	ENSP00000353393.4:n.-154T=
ENST00000647125.1:c.-154T=	ENSP00000496062.1:n.-154T=
ENST00000360256.8:c.-154T=	ENSP00000353393.4:n.-154T=
ENST00000423959.5:c.38+4074T=	ENSP00000409446.1:n.38+4074T=
ENST00000453950.1:c.39-210T=	ENSP00000389153.1:n.39-210T=
NM_000132.3:c.-154T=	NP_000123.1:n.-154T=
XM_011531126.1:c.38+4074T=	XP_011529428.1:n.38+4074T=
NM_000132.4:c.-154T= MANE Select	NP_000123.1:n.-154T=