Canonical Allele Identifier: CA2466865407

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022414C= , CM000685.2:g.155022414C=	GRCh38
NC_000023.10:g.154250689C= , CM000685.1:g.154250689C=	GRCh37
NC_000023.9:g.153903883C=	NCBI36
NG_011403.1:g.5310G=
NG_011403.2:g.5310G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.139G= MANE Select	ENSP00000353393.4:p.Ala47=
ENST00000647125.1:c.121+18G=	ENSP00000496062.1:n.121+18G=
ENST00000360256.8:c.139G=	ENSP00000353393.4:p.Ala47=
ENST00000423959.5:c.38+4366G=	ENSP00000409446.1:n.38+4366G=
ENST00000453950.1:c.121G=	ENSP00000389153.1:p.Ala41=
NM_000132.3:c.139G=	NP_000123.1:p.Ala47=
XM_011531126.1:c.38+4366G=	XP_011529428.1:n.38+4366G=
NM_000132.4:c.139G= MANE Select	NP_000123.1:p.Ala47=