Canonical Allele Identifier: CA585122941
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1432487119
gnomAD v2: 8-129559376-AGTGTGT-A
gnomAD v3: 8-128547130-AGTGTGT-A
gnomAD v4: 8-128547130-AGTGTGT-A
MyVariant Identifiers: chr8:g.129559377_129559382del (hg19) chr8:g.128547131_128547136del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547131_128547136del , CM000670.2:g.128547131_128547136del GRCh38
NC_000008.10:g.129559377_129559382del , CM000670.1:g.129559377_129559382del GRCh37
NC_000008.9:g.129628559_129628564del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13934_508+13939del
Search 100 bp 5'
Search 100 bp 3'