Canonical Allele Identifier: CA2466846508

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154961153G= , CM000685.2:g.154961153G=	GRCh38
NC_000023.10:g.154189428G= , CM000685.1:g.154189428G=	GRCh37
NC_000023.9:g.153842622G=	NCBI36
NG_011403.1:g.66571C=
NG_011403.2:g.66571C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1459C= MANE Select	ENSP00000353393.4:p.Gln487=
ENST00000647125.1:c.*1335C=	ENSP00000496062.1:n.*1335C=
ENST00000360256.8:c.1459C=	ENSP00000353393.4:p.Gln487=
NM_000132.3:c.1459C=	NP_000123.1:p.Gln487=
XM_011531126.1:c.1354C=	XP_011529428.1:p.Gln452=
NM_000132.4:c.1459C= MANE Select	NP_000123.1:p.Gln487=