Canonical Allele Identifier: CA425343849
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 3231481
ClinVar RCV Id: RCV004525552
dbSNP Id: rs1200318466
gnomAD v3: 2-21006998-G-T
gnomAD v4: 2-21006998-G-T
MyVariant Identifiers: chr2:g.21229870G>T (hg19) chr2:g.21006998G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006998G>T , CM000664.2:g.21006998G>T GRCh38
NC_000002.11:g.21229870G>T , CM000664.1:g.21229870G>T GRCh37
NC_000002.10:g.21083375G>T NCBI36
NG_011793.1:g.42076C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9870C>A MANE Select ENSP00000233242.1:p.Val3290=
ENST00000616098.4:c.9870C>A ENSP00000477990.1:p.Val3290=
NM_000384.2:c.9870C>A NP_000375.2:p.Val3290=
XM_011532809.1:c.5869+3735C>A XP_011531111.1:n.5869+3735C>A
NM_000384.3:c.9870C>A MANE Select NP_000375.3:p.Val3290=
Search 100 bp 5'
Search 100 bp 3'