Canonical Allele Identifier: CA346009168
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21015480G>T , CM000664.2:g.21015480G>T GRCh38
NC_000002.11:g.21238352G>T , CM000664.1:g.21238352G>T GRCh37
NC_000002.10:g.21091857G>T NCBI36
NG_011793.1:g.33594C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*2704C>A ENSP00000501110.2:n.*2704C>A
ENST00000673882.2:c.*2493C>A ENSP00000501253.2:n.*2493C>A
ENST00000673739.1:c.3112C>A ENSP00000501110.1:n.3112C>A
ENST00000673882.1:c.2901C>A ENSP00000501253.1:n.2901C>A
ENST00000233242.5:c.3398C>A MANE Select ENSP00000233242.1:p.Ala1133Asp
ENST00000616098.4:c.3398C>A ENSP00000477990.1:p.Ala1133Asp
NM_000384.2:c.3398C>A NP_000375.2:p.Ala1133Asp
XM_011532809.1:c.3398C>A XP_011531111.1:p.Ala1133Asp
NM_000384.3:c.3398C>A MANE Select NP_000375.3:p.Ala1133Asp