Canonical Allele Identifier: CA425121025

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21260875G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038003G>T , CM000664.2:g.21038003G>T	GRCh38
NC_000002.11:g.21260875G>T , CM000664.1:g.21260875G>T	GRCh37
NC_000002.10:g.21114380G>T	NCBI36
NG_011793.1:g.11071C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.384-748C>A	ENSP00000501110.2:n.384-748C>A
ENST00000673882.2:c.384-748C>A	ENSP00000501253.2:n.384-748C>A
ENST00000673739.1:c.252-748C>A	ENSP00000501110.1:n.252-748C>A
ENST00000673882.1:c.252-748C>A	ENSP00000501253.1:n.252-748C>A
ENST00000233242.5:c.492C>A MANE Select	ENSP00000233242.1:p.Leu164=
ENST00000399256.4:c.492C>A	ENSP00000382200.4:p.Leu164=
ENST00000616098.4:c.492C>A	ENSP00000477990.1:p.Leu164=
NM_000384.2:c.492C>A	NP_000375.2:p.Leu164=
XM_011532809.1:c.492C>A	XP_011531111.1:p.Leu164=
NM_000384.3:c.492C>A MANE Select	NP_000375.3:p.Leu164=