Canonical Allele Identifier: CA2576686510
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21006953-T-TGGC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006954_21006956dup , CM000664.2:g.21006954_21006956dup GRCh38
NC_000002.11:g.21229826_21229828dup , CM000664.1:g.21229826_21229828dup GRCh37
NC_000002.10:g.21083331_21083333dup NCBI36
NG_011793.1:g.42118_42120dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9912_9914dup MANE Select ENSP00000233242.1:p.Pro3305_Val3306insPro
ENST00000616098.4:c.9912_9914dup ENSP00000477990.1:p.Pro3305_Val3306insPro
NM_000384.2:c.9912_9914dup NP_000375.2:p.Pro3305_Val3306insPro
XM_011532809.1:c.5869+3777_5869+3779dup XP_011531111.1:n.5869+3777_5869+3779dup
NM_000384.3:c.9912_9914dup MANE Select NP_000375.3:p.Pro3305_Val3306insPro
Search 100 bp 5'
Search 100 bp 3'