Canonical Allele Identifier: CA2466865419

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022451G= , CM000685.2:g.155022451G=	GRCh38
NC_000023.10:g.154250726G= , CM000685.1:g.154250726G=	GRCh37
NC_000023.9:g.153903920G=	NCBI36
NG_011403.1:g.5273C=
NG_011403.2:g.5273C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.102C= MANE Select	ENSP00000353393.4:p.Asp34=
ENST00000647125.1:c.102C=	ENSP00000496062.1:p.Asp34=
ENST00000360256.8:c.102C=	ENSP00000353393.4:p.Asp34=
ENST00000423959.5:c.38+4329C=	ENSP00000409446.1:n.38+4329C=
ENST00000453950.1:c.84C=	ENSP00000389153.1:p.Asp28=
NM_000132.3:c.102C=	NP_000123.1:p.Asp34=
XM_011531126.1:c.38+4329C=	XP_011529428.1:n.38+4329C=
NM_000132.4:c.102C= MANE Select	NP_000123.1:p.Asp34=