Canonical Allele Identifier: CA1028216546
Gene: APOB HGNC NCBI

Linked Data

gnomAD v3: 2-21023464-A-AAGAAATGCACCCTGGAAGAAAGTAATAACCTAAGAAATCAAAAGGC
gnomAD v4: 2-21023464-A-AAGAAATGCACCCTGGAAGAAAGTAATAACCTAAGAAATCAAAAGGC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21023466_21023511dup , CM000664.2:g.21023466_21023511dup GRCh38
NC_000002.11:g.21246338_21246383dup , CM000664.1:g.21246338_21246383dup GRCh37
NC_000002.10:g.21099843_21099888dup NCBI36
NG_011793.1:g.25564_25609dup

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.*1910+15_*1910+60dup ENSP00000501110.2:n.*1910+15_*1910+60dup
ENST00000673882.2:c.*1910+15_*1910+60dup ENSP00000501253.2:n.*1910+15_*1910+60dup
ENST00000673739.1:c.2318+15_2318+60dup ENSP00000501110.1:n.2318+15_2318+60dup
ENST00000673882.1:c.2318+15_2318+60dup ENSP00000501253.1:n.2318+15_2318+60dup
ENST00000233242.5:c.2604+15_2604+60dup MANE Select ENSP00000233242.1:n.2604+15_2604+60dup
ENST00000616098.4:c.2604+15_2604+60dup ENSP00000477990.1:n.2604+15_2604+60dup
NM_000384.2:c.2604+15_2604+60dup NP_000375.2:n.2604+15_2604+60dup
XM_011532809.1:c.2604+15_2604+60dup XP_011531111.1:n.2604+15_2604+60dup
NM_000384.3:c.2604+15_2604+60dup MANE Select NP_000375.3:n.2604+15_2604+60dup
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