Canonical Allele Identifier: CA425346117
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21010928-G-T
MyVariant Identifiers: chr2:g.21233800G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010928G>T , CM000664.2:g.21010928G>T GRCh38
NC_000002.11:g.21233800G>T , CM000664.1:g.21233800G>T GRCh37
NC_000002.10:g.21087305G>T NCBI36
NG_011793.1:g.38146C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5940C>A MANE Select ENSP00000233242.1:p.Thr1980=
ENST00000616098.4:c.5940C>A ENSP00000477990.1:p.Thr1980=
NM_000384.2:c.5940C>A NP_000375.2:p.Thr1980=
XM_011532809.1:c.5864+76C>A XP_011531111.1:n.5864+76C>A
NM_000384.3:c.5940C>A MANE Select NP_000375.3:p.Thr1980=
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