Canonical Allele Identifier: CA346009212
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21015501A>G , CM000664.2:g.21015501A>G GRCh38
NC_000002.11:g.21238373A>G , CM000664.1:g.21238373A>G GRCh37
NC_000002.10:g.21091878A>G NCBI36
NG_011793.1:g.33573T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*2683T>C ENSP00000501110.2:n.*2683T>C
ENST00000673882.2:c.*2472T>C ENSP00000501253.2:n.*2472T>C
ENST00000673739.1:c.3091T>C ENSP00000501110.1:n.3091T>C
ENST00000673882.1:c.2880T>C ENSP00000501253.1:n.2880T>C
ENST00000233242.5:c.3377T>C MANE Select ENSP00000233242.1:p.Ile1126Thr
ENST00000616098.4:c.3377T>C ENSP00000477990.1:p.Ile1126Thr
NM_000384.2:c.3377T>C NP_000375.2:p.Ile1126Thr
XM_011532809.1:c.3377T>C XP_011531111.1:p.Ile1126Thr
NM_000384.3:c.3377T>C MANE Select NP_000375.3:p.Ile1126Thr