Canonical Allele Identifier: CA2466835736

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154928589G= , CM000685.2:g.154928589G=	GRCh38
NC_000023.10:g.154156864G= , CM000685.1:g.154156864G=	GRCh37
NC_000023.9:g.153810058G=	NCBI36
NG_011403.1:g.99135C=
NG_011403.2:g.99135C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.5201C= MANE Select	ENSP00000353393.4:p.Pro1734=
ENST00000360256.8:c.5201C=	ENSP00000353393.4:p.Pro1734=
NM_000132.3:c.5201C=	NP_000123.1:p.Pro1734=
XM_011531126.1:c.5096C=	XP_011529428.1:p.Pro1699=
NM_000132.4:c.5201C= MANE Select	NP_000123.1:p.Pro1734=