Canonical Allele Identifier: CA345969888
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21225295G>C (hg19) chr2:g.21002423G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002423G>C , CM000664.2:g.21002423G>C GRCh38
NC_000002.11:g.21225295G>C , CM000664.1:g.21225295G>C GRCh37
NC_000002.10:g.21078800G>C NCBI36
NG_011793.1:g.46651C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.12999C>G MANE Select ENSP00000233242.1:p.Ile4333Met
ENST00000616098.4:c.12999C>G ENSP00000477990.1:p.Ile4333Met
NM_000384.2:c.12999C>G NP_000375.2:p.Ile4333Met
XM_011532809.1:c.5870-3150C>G XP_011531111.1:n.5870-3150C>G
NM_000384.3:c.12999C>G MANE Select NP_000375.3:p.Ile4333Met
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