Canonical Allele Identifier: CA2658076740
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21007578-T-TTA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007581_21007582dup , CM000664.2:g.21007581_21007582dup GRCh38
NC_000002.11:g.21230453_21230454dup , CM000664.1:g.21230453_21230454dup GRCh37
NC_000002.10:g.21083958_21083959dup NCBI36
NG_011793.1:g.41494_41495dup

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.9288_9289dup MANE Select ENSP00000233242.1:p.Lys3097IlefsTer20
ENST00000616098.4:c.9288_9289dup ENSP00000477990.1:p.Lys3097IlefsTer20
NM_000384.2:c.9288_9289dup NP_000375.2:p.Lys3097IlefsTer20
XM_011532809.1:c.5869+3153_5869+3154dup XP_011531111.1:n.5869+3153_5869+3154dup
NM_000384.3:c.9288_9289dup MANE Select NP_000375.3:p.Lys3097IlefsTer20
Search 100 bp 5'
Search 100 bp 3'