Canonical Allele Identifier: CA2493478077

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21013297G= , CM000664.2:g.21013297G=	GRCh38
NC_000002.11:g.21236169G= , CM000664.1:g.21236169G=	GRCh37
NC_000002.10:g.21089674G=	NCBI36
NG_011793.1:g.35777C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.*3385C=	ENSP00000501110.2:n.*3385C=
ENST00000673739.1:c.3793C=	ENSP00000501110.1:n.3793C=
ENST00000233242.5:c.4079C= MANE Select	ENSP00000233242.1:p.Thr1360=
ENST00000616098.4:c.4079C=	ENSP00000477990.1:p.Thr1360=
NM_000384.2:c.4079C=	NP_000375.2:p.Thr1360=
XM_011532809.1:c.4079C=	XP_011531111.1:p.Thr1360=
NM_000384.3:c.4079C= MANE Select	NP_000375.3:p.Thr1360=