Canonical Allele Identifier: CA43465979

Gene: APOB

Linked Data

• dbSNP Id: rs755523155
• gnomAD v2: 2-21261251-C-T
• gnomAD v3: 2-21038379-C-T
• gnomAD v4: 2-21038379-C-T
• MyVariant Identifiers: chr2:g.21261251C>T (hg19) ; chr2:g.21038379C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038379C>T , CM000664.2:g.21038379C>T	GRCh38
NC_000002.11:g.21261251C>T , CM000664.1:g.21261251C>T	GRCh37
NC_000002.10:g.21114756C>T	NCBI36
NG_011793.1:g.10695G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-1124G>A	ENSP00000501110.2:n.384-1124G>A
ENST00000673882.2:c.384-1124G>A	ENSP00000501253.2:n.384-1124G>A
ENST00000673739.1:c.252-1124G>A	ENSP00000501110.1:n.252-1124G>A
ENST00000673882.1:c.252-1124G>A	ENSP00000501253.1:n.252-1124G>A
ENST00000233242.5:c.384-268G>A MANE Select	ENSP00000233242.1:n.384-268G>A
ENST00000399256.4:c.384-268G>A	ENSP00000382200.4:n.384-268G>A
ENST00000616098.4:c.384-268G>A	ENSP00000477990.1:n.384-268G>A
NM_000384.2:c.384-268G>A	NP_000375.2:n.384-268G>A
XM_011532809.1:c.384-268G>A	XP_011531111.1:n.384-268G>A
NM_000384.3:c.384-268G>A MANE Select	NP_000375.3:n.384-268G>A