Canonical Allele Identifier: CA2466865511

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022709T= , CM000685.2:g.155022709T=	GRCh38
NC_000023.10:g.154250984T= , CM000685.1:g.154250984T=	GRCh37
NC_000023.9:g.153904178T=	NCBI36
NG_011403.1:g.5015A=
NG_011403.2:g.5015A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-157A= MANE Select	ENSP00000353393.4:n.-157A=
ENST00000647125.1:c.-157A=	ENSP00000496062.1:n.-157A=
ENST00000360256.8:c.-157A=	ENSP00000353393.4:n.-157A=
ENST00000423959.5:c.38+4071A=	ENSP00000409446.1:n.38+4071A=
ENST00000453950.1:c.39-213A=	ENSP00000389153.1:n.39-213A=
NM_000132.3:c.-157A=	NP_000123.1:n.-157A=
XM_011531126.1:c.38+4071A=	XP_011529428.1:n.38+4071A=
NM_000132.4:c.-157A= MANE Select	NP_000123.1:n.-157A=