Canonical Allele Identifier: CA2466827669

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902188C= , CM000685.2:g.154902188C=	GRCh38
NC_000023.10:g.154130463C= , CM000685.1:g.154130463C=	GRCh37
NC_000023.9:g.153783657C=	NCBI36
NG_011403.1:g.125536G=
NG_011403.2:g.125536G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5999-21G= MANE Select	ENSP00000353393.4:n.5999-21G=
ENST00000360256.8:c.5999-21G=	ENSP00000353393.4:n.5999-21G=
NM_000132.3:c.5999-21G=	NP_000123.1:n.5999-21G=
XM_011531126.1:c.5894-21G=	XP_011529428.1:n.5894-21G=
NM_000132.4:c.5999-21G= MANE Select	NP_000123.1:n.5999-21G=