Canonical Allele Identifier: CA1119097443
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816087331
gnomAD v3: 8-128529830-G-A
gnomAD v4: 8-128529830-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529830G>A , CM000670.2:g.128529830G>A GRCh38
NC_000008.10:g.129542076G>A , CM000670.1:g.129542076G>A GRCh37
NC_000008.9:g.129611258G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31240C>T
Search 100 bp 5'
Search 100 bp 3'