Canonical Allele Identifier: CA2466865363

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022293T= , CM000685.2:g.155022293T=	GRCh38
NC_000023.10:g.154250568T= , CM000685.1:g.154250568T=	GRCh37
NC_000023.9:g.153903762T=	NCBI36
NG_011403.1:g.5431A=
NG_011403.2:g.5431A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.143+117A= MANE Select	ENSP00000353393.4:n.143+117A=
ENST00000647125.1:c.121+139A=	ENSP00000496062.1:n.121+139A=
ENST00000360256.8:c.143+117A=	ENSP00000353393.4:n.143+117A=
ENST00000423959.5:c.38+4487A=	ENSP00000409446.1:n.38+4487A=
ENST00000453950.1:c.125+117A=	ENSP00000389153.1:n.125+117A=
NM_000132.3:c.143+117A=	NP_000123.1:n.143+117A=
XM_011531126.1:c.38+4487A=	XP_011529428.1:n.38+4487A=
NM_000132.4:c.143+117A= MANE Select	NP_000123.1:n.143+117A=