Canonical Allele Identifier: CA345970068
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21002462-C-T
COSMIC: COSM5526772
MyVariant Identifiers: chr2:g.21225334C>T (hg19) chr2:g.21002462C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002462C>T , CM000664.2:g.21002462C>T GRCh38
NC_000002.11:g.21225334C>T , CM000664.1:g.21225334C>T GRCh37
NC_000002.10:g.21078839C>T NCBI36
NG_011793.1:g.46612G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.12960G>A MANE Select ENSP00000233242.1:p.Met4320Ile
ENST00000616098.4:c.12960G>A ENSP00000477990.1:p.Met4320Ile
NM_000384.2:c.12960G>A NP_000375.2:p.Met4320Ile
XM_011532809.1:c.5870-3189G>A XP_011531111.1:n.5870-3189G>A
NM_000384.3:c.12960G>A MANE Select NP_000375.3:p.Met4320Ile
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