Canonical Allele Identifier: CA2658054391
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21001651-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001651A>G , CM000664.2:g.21001651A>G GRCh38
NC_000002.11:g.21224523A>G , CM000664.1:g.21224523A>G GRCh37
NC_000002.10:g.21078028A>G NCBI36
NG_011793.1:g.47423T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*79T>C MANE Select ENSP00000233242.1:n.*79T>C
ENST00000616098.4:c.13769T>C ENSP00000477990.1:n.13769T>C
NM_000384.2:c.*79T>C NP_000375.2:n.*79T>C
XM_011532809.1:c.5870-2378T>C XP_011531111.1:n.5870-2378T>C
NM_000384.3:c.*79T>C MANE Select NP_000375.3:n.*79T>C
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