Canonical Allele Identifier: CA1119101086
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs34606099
gnomAD v3: 8-128547095-C-CAAAAAAAAAAAAAAAAAAAAAAA
gnomAD v4: 8-128547095-C-CAAAAAAAAAAAAAAAAAAAAAAA
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547114_128547115insAAAAAAAAAAAAAAAAAAAAAAA , CM000670.2:g.128547114_128547115insAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000008.10:g.129559360_129559361insAAAAAAAAAAAAAAAAAAAAAAA , CM000670.1:g.129559360_129559361insAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000008.9:g.129628542_129628543insAAAAAAAAAAAAAAAAAAAAAAA NCBI36

Transcript Alleles

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