Canonical Allele Identifier: CA346007664
Gene: APOB HGNC NCBI

Linked Data

COSMIC: COSM3372630
MyVariant Identifiers: chr2:g.21236165A>T (hg19) chr2:g.21013293A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21013293A>T , CM000664.2:g.21013293A>T GRCh38
NC_000002.11:g.21236165A>T , CM000664.1:g.21236165A>T GRCh37
NC_000002.10:g.21089670A>T NCBI36
NG_011793.1:g.35781T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*3389T>A ENSP00000501110.2:n.*3389T>A
ENST00000673739.1:c.3797T>A ENSP00000501110.1:n.3797T>A
ENST00000233242.5:c.4083T>A MANE Select ENSP00000233242.1:p.Asn1361Lys
ENST00000616098.4:c.4083T>A ENSP00000477990.1:p.Asn1361Lys
NM_000384.2:c.4083T>A NP_000375.2:p.Asn1361Lys
XM_011532809.1:c.4083T>A XP_011531111.1:p.Asn1361Lys
NM_000384.3:c.4083T>A MANE Select NP_000375.3:p.Asn1361Lys
Search 100 bp 5'
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