Canonical Allele Identifier: CA346003564
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21233762C>G (hg19) chr2:g.21010890C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010890C>G , CM000664.2:g.21010890C>G GRCh38
NC_000002.11:g.21233762C>G , CM000664.1:g.21233762C>G GRCh37
NC_000002.10:g.21087267C>G NCBI36
NG_011793.1:g.38184G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5978G>C MANE Select ENSP00000233242.1:p.Ser1993Thr
ENST00000616098.4:c.5978G>C ENSP00000477990.1:p.Ser1993Thr
NM_000384.2:c.5978G>C NP_000375.2:p.Ser1993Thr
XM_011532809.1:c.5864+114G>C XP_011531111.1:n.5864+114G>C
NM_000384.3:c.5978G>C MANE Select NP_000375.3:p.Ser1993Thr
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