Canonical Allele Identifier: CA1119101133
Gene: LINC00824 HGNC NCBI

Linked Data

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

HGVS Genome Assembly
NC_000008.11:g.128547114_128547115insAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000670.2:g.128547114_128547115insAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000008.10:g.129559360_129559361insAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000670.1:g.129559360_129559361insAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000008.9:g.129628542_129628543insAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NCBI36

Transcript Alleles

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