Canonical Allele Identifier: CA1119097880
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816119291
gnomAD v3: 8-128531654-C-T
gnomAD v4: 8-128531654-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531654C>T , CM000670.2:g.128531654C>T GRCh38
NC_000008.10:g.129543900C>T , CM000670.1:g.129543900C>T GRCh37
NC_000008.9:g.129613082C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29416G>A
Search 100 bp 5'
Search 100 bp 3'