Canonical Allele Identifier: CA43466026

Gene: APOB

Linked Data

• dbSNP Id: rs906951898
• MyVariant Identifiers: chr2:g.21261296C>A (hg19) ; chr2:g.21038424C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038424C>A , CM000664.2:g.21038424C>A	GRCh38
NC_000002.11:g.21261296C>A , CM000664.1:g.21261296C>A	GRCh37
NC_000002.10:g.21114801C>A	NCBI36
NG_011793.1:g.10650G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-1169G>T	ENSP00000501110.2:n.384-1169G>T
ENST00000673882.2:c.384-1169G>T	ENSP00000501253.2:n.384-1169G>T
ENST00000673739.1:c.252-1169G>T	ENSP00000501110.1:n.252-1169G>T
ENST00000673882.1:c.252-1169G>T	ENSP00000501253.1:n.252-1169G>T
ENST00000233242.5:c.384-313G>T MANE Select	ENSP00000233242.1:n.384-313G>T
ENST00000399256.4:c.384-313G>T	ENSP00000382200.4:n.384-313G>T
ENST00000616098.4:c.384-313G>T	ENSP00000477990.1:n.384-313G>T
NM_000384.2:c.384-313G>T	NP_000375.2:n.384-313G>T
XM_011532809.1:c.384-313G>T	XP_011531111.1:n.384-313G>T
NM_000384.3:c.384-313G>T MANE Select	NP_000375.3:n.384-313G>T