Canonical Allele Identifier: CA345962514

Gene: APOB

Linked Data

• gnomAD v4: 2-21037992-G-C
• MyVariant Identifiers: chr2:g.21260864G>C (hg19) ; chr2:g.21037992G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21037992G>C , CM000664.2:g.21037992G>C	GRCh38
NC_000002.11:g.21260864G>C , CM000664.1:g.21260864G>C	GRCh37
NC_000002.10:g.21114369G>C	NCBI36
NG_011793.1:g.11082C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.384-737C>G	ENSP00000501110.2:n.384-737C>G
ENST00000673882.2:c.384-737C>G	ENSP00000501253.2:n.384-737C>G
ENST00000673739.1:c.252-737C>G	ENSP00000501110.1:n.252-737C>G
ENST00000673882.1:c.252-737C>G	ENSP00000501253.1:n.252-737C>G
ENST00000233242.5:c.503C>G MANE Select	ENSP00000233242.1:p.Pro168Arg
ENST00000399256.4:c.503C>G	ENSP00000382200.4:p.Pro168Arg
ENST00000616098.4:c.503C>G	ENSP00000477990.1:p.Pro168Arg
NM_000384.2:c.503C>G	NP_000375.2:p.Pro168Arg
XM_011532809.1:c.503C>G	XP_011531111.1:p.Pro168Arg
NM_000384.3:c.503C>G MANE Select	NP_000375.3:p.Pro168Arg