Canonical Allele Identifier: CA1119100961
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816377106
gnomAD v3: 8-128547095-C-CAAAAAAAAATAAATAAA
gnomAD v4: 8-128547095-C-CAAAAAAAAATAAATAAA
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547104_128547105insTAAATAAAAAAAAAAAA , CM000670.2:g.128547104_128547105insTAAATAAAAAAAAAAAA GRCh38
NC_000008.10:g.129559350_129559351insTAAATAAAAAAAAAAAA , CM000670.1:g.129559350_129559351insTAAATAAAAAAAAAAAA GRCh37
NC_000008.9:g.129628532_129628533insTAAATAAAAAAAAAAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13974_508+13975insTTTATTTATTTTTTTTT
Search 100 bp 5'
Search 100 bp 3'