Canonical Allele Identifier: CA2466826085

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896353G= , CM000685.2:g.154896353G=	GRCh38
NC_000023.10:g.154124628G= , CM000685.1:g.154124628G=	GRCh37
NC_000023.9:g.153777822G=	NCBI36
NG_011403.1:g.131371C=
NG_011403.2:g.131371C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6274-121C= MANE Select	ENSP00000353393.4:n.6274-121C=
ENST00000360256.8:c.6274-121C=	ENSP00000353393.4:n.6274-121C=
NM_000132.3:c.6274-121C=	NP_000123.1:n.6274-121C=
XM_011531126.1:c.6169-121C=	XP_011529428.1:n.6169-121C=
NM_000132.4:c.6274-121C= MANE Select	NP_000123.1:n.6274-121C=