Canonical Allele Identifier: CA2466846480

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154961079T= , CM000685.2:g.154961079T=	GRCh38
NC_000023.10:g.154189354T= , CM000685.1:g.154189354T=	GRCh37
NC_000023.9:g.153842548T=	NCBI36
NG_011403.1:g.66645A=
NG_011403.2:g.66645A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1533A= MANE Select	ENSP00000353393.4:p.Pro511=
ENST00000647125.1:c.*1409A=	ENSP00000496062.1:n.*1409A=
ENST00000360256.8:c.1533A=	ENSP00000353393.4:p.Pro511=
NM_000132.3:c.1533A=	NP_000123.1:p.Pro511=
XM_011531126.1:c.1428A=	XP_011529428.1:p.Pro476=
NM_000132.4:c.1533A= MANE Select	NP_000123.1:p.Pro511=