Canonical Allele Identifier: CA346004478
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2487702
ClinVar RCV Id: RCV004273348
MyVariant Identifiers: chr2:g.21234188T>G (hg19) chr2:g.21011316T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011316T>G , CM000664.2:g.21011316T>G GRCh38
NC_000002.11:g.21234188T>G , CM000664.1:g.21234188T>G GRCh37
NC_000002.10:g.21087693T>G NCBI36
NG_011793.1:g.37758A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5552A>C MANE Select ENSP00000233242.1:p.Tyr1851Ser
ENST00000616098.4:c.5552A>C ENSP00000477990.1:p.Tyr1851Ser
NM_000384.2:c.5552A>C NP_000375.2:p.Tyr1851Ser
XM_011532809.1:c.5552A>C XP_011531111.1:p.Tyr1851Ser
NM_000384.3:c.5552A>C MANE Select NP_000375.3:p.Tyr1851Ser
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