Canonical Allele Identifier: CA2604623182
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816093288
gnomAD v3: 8-128530189-C-T
gnomAD v4: 8-128530189-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530189C>T , CM000670.2:g.128530189C>T GRCh38
NC_000008.10:g.129542435C>T , CM000670.1:g.129542435C>T GRCh37
NC_000008.9:g.129611617C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30881G>A
Search 100 bp 5'
Search 100 bp 3'