Canonical Allele Identifier: CA585122927
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816378056
gnomAD v2: 8-129559360-ATAG-A
gnomAD v3: 8-128547114-ATAG-A
gnomAD v4: 8-128547114-ATAG-A
MyVariant Identifiers: chr8:g.129559361_129559365delinsAG (hg19) chr8:g.128547115_128547119delinsAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547115_128547117del , CM000670.2:g.128547115_128547117del GRCh38
NC_000008.10:g.129559361_129559363del , CM000670.1:g.129559361_129559363del GRCh37
NC_000008.9:g.129628543_129628545del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13953_508+13955del
Search 100 bp 5'
Search 100 bp 3'