Canonical Allele Identifier: CA1119100817
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816372486
gnomAD v3: 8-128546882-T-A
gnomAD v4: 8-128546882-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546882T>A , CM000670.2:g.128546882T>A GRCh38
NC_000008.10:g.129559128T>A , CM000670.1:g.129559128T>A GRCh37
NC_000008.9:g.129628310T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14188A>T
Search 100 bp 5'
Search 100 bp 3'