Canonical Allele Identifier: CA2466865447

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022527A= , CM000685.2:g.155022527A=	GRCh38
NC_000023.10:g.154250802A= , CM000685.1:g.154250802A=	GRCh37
NC_000023.9:g.153903996A=	NCBI36
NG_011403.1:g.5197T=
NG_011403.2:g.5197T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.26T= MANE Select	ENSP00000353393.4:p.Phe9=
ENST00000647125.1:c.26T=	ENSP00000496062.1:p.Phe9=
ENST00000360256.8:c.26T=	ENSP00000353393.4:p.Phe9=
ENST00000423959.5:c.38+4253T=	ENSP00000409446.1:n.38+4253T=
ENST00000453950.1:c.39-31T=	ENSP00000389153.1:n.39-31T=
NM_000132.3:c.26T=	NP_000123.1:p.Phe9=
XM_011531126.1:c.38+4253T=	XP_011529428.1:n.38+4253T=
NM_000132.4:c.26T= MANE Select	NP_000123.1:p.Phe9=