Canonical Allele Identifier: CA585122939
Gene: LINC00824 HGNC NCBI

Linked Data

gnomAD v2: 8-129559374-C-CAAAA
gnomAD v3: 8-128547128-C-CAAAA
gnomAD v4: 8-128547128-C-CAAAA
MyVariant Identifiers: chr8:g.129559374_129559375insAAAA (hg19) chr8:g.128547128_128547129insAAAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547130_128547131insAAAA , CM000670.2:g.128547130_128547131insAAAA GRCh38
NC_000008.10:g.129559376_129559377insAAAA , CM000670.1:g.129559376_129559377insAAAA GRCh37
NC_000008.9:g.129628558_129628559insAAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13941_508+13942insTTTT
Search 100 bp 5'
Search 100 bp 3'