Canonical Allele Identifier: CA915700834
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1563629735
gnomAD v2: 8-129542384-TAGGCTCATGCAGCCTCCGCCTCCC-T
gnomAD v3: 8-128530138-TAGGCTCATGCAGCCTCCGCCTCCC-T
gnomAD v4: 8-128530138-TAGGCTCATGCAGCCTCCGCCTCCC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530142_128530165del , CM000670.2:g.128530142_128530165del GRCh38
NC_000008.10:g.129542388_129542411del , CM000670.1:g.129542388_129542411del GRCh37
NC_000008.9:g.129611570_129611593del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30908_508+30931del
Search 100 bp 5'
Search 100 bp 3'