Canonical Allele Identifier: CA463033625
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816376925
gnomAD v2: 8-129559340-G-GAAA
gnomAD v3: 8-128547094-G-GAAA
gnomAD v4: 8-128547094-G-GAAA
MyVariant Identifiers: chr8:g.129559340_129559341insAAA (hg19) chr8:g.128547094_128547095insAAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547094_128547095insAAA , CM000670.2:g.128547094_128547095insAAA GRCh38
NC_000008.10:g.129559340_129559341insAAA , CM000670.1:g.129559340_129559341insAAA GRCh37
NC_000008.9:g.129628522_129628523insAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13975_508+13976insTTT
Search 100 bp 5'
Search 100 bp 3'