Canonical Allele Identifier: CA2493479059

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015498G= , CM000664.2:g.21015498G=	GRCh38
NC_000002.11:g.21238370G= , CM000664.1:g.21238370G=	GRCh37
NC_000002.10:g.21091875G=	NCBI36
NG_011793.1:g.33576C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2686C=	ENSP00000501110.2:n.*2686C=
ENST00000673882.2:c.*2475C=	ENSP00000501253.2:n.*2475C=
ENST00000673739.1:c.3094C=	ENSP00000501110.1:n.3094C=
ENST00000673882.1:c.2883C=	ENSP00000501253.1:n.2883C=
ENST00000233242.5:c.3380C= MANE Select	ENSP00000233242.1:p.Pro1127=
ENST00000616098.4:c.3380C=	ENSP00000477990.1:p.Pro1127=
NM_000384.2:c.3380C=	NP_000375.2:p.Pro1127=
XM_011532809.1:c.3380C=	XP_011531111.1:p.Pro1127=
NM_000384.3:c.3380C= MANE Select	NP_000375.3:p.Pro1127=