Canonical Allele Identifier: CA2466836701

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154931489G= , CM000685.2:g.154931489G=	GRCh38
NC_000023.10:g.154159764G= , CM000685.1:g.154159764G=	GRCh37
NC_000023.9:g.153812958G=	NCBI36
NG_011403.1:g.96235C=
NG_011403.2:g.96235C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.2301C= MANE Select	ENSP00000353393.4:p.His767=
ENST00000647125.1:c.*1967C=	ENSP00000496062.1:n.*1967C=
ENST00000360256.8:c.2301C=	ENSP00000353393.4:p.His767=
NM_000132.3:c.2301C=	NP_000123.1:p.His767=
XM_011531126.1:c.2196C=	XP_011529428.1:p.His732=
NM_000132.4:c.2301C= MANE Select	NP_000123.1:p.His767=