Canonical Allele Identifier: CA425136555

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21238342C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015470C>T , CM000664.2:g.21015470C>T	GRCh38
NC_000002.11:g.21238342C>T , CM000664.1:g.21238342C>T	GRCh37
NC_000002.10:g.21091847C>T	NCBI36
NG_011793.1:g.33604G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2714G>A	ENSP00000501110.2:n.*2714G>A
ENST00000673882.2:c.*2503G>A	ENSP00000501253.2:n.*2503G>A
ENST00000673739.1:c.3122G>A	ENSP00000501110.1:n.3122G>A
ENST00000673882.1:c.2911G>A	ENSP00000501253.1:n.2911G>A
ENST00000233242.5:c.3408G>A MANE Select	ENSP00000233242.1:p.Glu1136=
ENST00000616098.4:c.3408G>A	ENSP00000477990.1:p.Glu1136=
NM_000384.2:c.3408G>A	NP_000375.2:p.Glu1136=
XM_011532809.1:c.3408G>A	XP_011531111.1:p.Glu1136=
NM_000384.3:c.3408G>A MANE Select	NP_000375.3:p.Glu1136=