Canonical Allele Identifier: CA2576686790
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21023459-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21023459T>C , CM000664.2:g.21023459T>C GRCh38
NC_000002.11:g.21246331T>C , CM000664.1:g.21246331T>C GRCh37
NC_000002.10:g.21099836T>C NCBI36
NG_011793.1:g.25615A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.*1910+66A>G ENSP00000501110.2:n.*1910+66A>G
ENST00000673882.2:c.*1910+66A>G ENSP00000501253.2:n.*1910+66A>G
ENST00000673739.1:c.2318+66A>G ENSP00000501110.1:n.2318+66A>G
ENST00000673882.1:c.2318+66A>G ENSP00000501253.1:n.2318+66A>G
ENST00000233242.5:c.2604+66A>G MANE Select ENSP00000233242.1:n.2604+66A>G
ENST00000616098.4:c.2604+66A>G ENSP00000477990.1:n.2604+66A>G
NM_000384.2:c.2604+66A>G NP_000375.2:n.2604+66A>G
XM_011532809.1:c.2604+66A>G XP_011531111.1:n.2604+66A>G
NM_000384.3:c.2604+66A>G MANE Select NP_000375.3:n.2604+66A>G