Canonical Allele Identifier: CA2658046622
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21023387-T-TA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21023394dup , CM000664.2:g.21023394dup GRCh38
NC_000002.11:g.21246266dup , CM000664.1:g.21246266dup GRCh37
NC_000002.10:g.21099771dup NCBI36
NG_011793.1:g.25686dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*1910+137dup ENSP00000501110.2:n.*1910+137dup
ENST00000673882.2:c.*1910+137dup ENSP00000501253.2:n.*1910+137dup
ENST00000673739.1:c.2318+137dup ENSP00000501110.1:n.2318+137dup
ENST00000673882.1:c.2318+137dup ENSP00000501253.1:n.2318+137dup
ENST00000233242.5:c.2604+137dup MANE Select ENSP00000233242.1:n.2604+137dup
ENST00000616098.4:c.2604+137dup ENSP00000477990.1:n.2604+137dup
NM_000384.2:c.2604+137dup NP_000375.2:n.2604+137dup
XM_011532809.1:c.2604+137dup XP_011531111.1:n.2604+137dup
NM_000384.3:c.2604+137dup MANE Select NP_000375.3:n.2604+137dup
Search 100 bp 5'
Search 100 bp 3'