Canonical Allele Identifier: CA345967425
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21224864A>T (hg19) chr2:g.21001992A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001992A>T , CM000664.2:g.21001992A>T GRCh38
NC_000002.11:g.21224864A>T , CM000664.1:g.21224864A>T GRCh37
NC_000002.10:g.21078369A>T NCBI36
NG_011793.1:g.47082T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13430T>A MANE Select ENSP00000233242.1:p.Ile4477Asn
ENST00000616098.4:c.13428T>A ENSP00000477990.1:n.13428T>A
NM_000384.2:c.13430T>A NP_000375.2:p.Ile4477Asn
XM_011532809.1:c.5870-2719T>A XP_011531111.1:n.5870-2719T>A
NM_000384.3:c.13430T>A MANE Select NP_000375.3:p.Ile4477Asn
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