Canonical Allele Identifier: CA43505650
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2930133
ClinVar RCV Id: RCV003787491
dbSNP Id: rs765661773
gnomAD v2: 2-21233589-C-G
gnomAD v4: 2-21010717-C-G
MyVariant Identifiers: chr2:g.21233589C>G (hg19) chr2:g.21010717C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010717C>G , CM000664.2:g.21010717C>G GRCh38
NC_000002.11:g.21233589C>G , CM000664.1:g.21233589C>G GRCh37
NC_000002.10:g.21087094C>G NCBI36
NG_011793.1:g.38357G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6151G>C MANE Select ENSP00000233242.1:p.Glu2051Gln
ENST00000616098.4:c.6151G>C ENSP00000477990.1:p.Glu2051Gln
NM_000384.2:c.6151G>C NP_000375.2:p.Glu2051Gln
XM_011532809.1:c.5869+16G>C XP_011531111.1:n.5869+16G>C
NM_000384.3:c.6151G>C MANE Select NP_000375.3:p.Glu2051Gln
Search 100 bp 5'
Search 100 bp 3'