Canonical Allele Identifier: CA1028204477
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1663158630
gnomAD v3: 2-21006863-GC-G
gnomAD v4: 2-21006863-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006866del , CM000664.2:g.21006866del GRCh38
NC_000002.11:g.21229738del , CM000664.1:g.21229738del GRCh37
NC_000002.10:g.21083243del NCBI36
NG_011793.1:g.42210del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.10004del MANE Select ENSP00000233242.1:p.Gly3335AlafsTer16
ENST00000616098.4:c.10004del ENSP00000477990.1:p.Gly3335AlafsTer16
NM_000384.2:c.10004del NP_000375.2:p.Gly3335AlafsTer16
XM_011532809.1:c.5869+3869del XP_011531111.1:n.5869+3869del
NM_000384.3:c.10004del MANE Select NP_000375.3:p.Gly3335AlafsTer16
Search 100 bp 5'
Search 100 bp 3'