Canonical Allele Identifier: CA2658054402
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21001673-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001673G>T , CM000664.2:g.21001673G>T GRCh38
NC_000002.11:g.21224545G>T , CM000664.1:g.21224545G>T GRCh37
NC_000002.10:g.21078050G>T NCBI36
NG_011793.1:g.47401C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*57C>A MANE Select ENSP00000233242.1:n.*57C>A
ENST00000616098.4:c.13747C>A ENSP00000477990.1:n.13747C>A
NM_000384.2:c.*57C>A NP_000375.2:n.*57C>A
XM_011532809.1:c.5870-2400C>A XP_011531111.1:n.5870-2400C>A
NM_000384.3:c.*57C>A MANE Select NP_000375.3:n.*57C>A
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