Canonical Allele Identifier: CA6058191
Gene: SNORD26 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs752593682
ExAC: 11:62622797 C / T
gnomAD v2: 11-62622797-C-T
gnomAD v4: 11-62855325-C-T
MyVariant Identifiers: chr11:g.62622797C>T (hg19) chr11:g.62855325C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855325C>T , CM000673.2:g.62855325C>T GRCh38
NC_000011.9:g.62622797C>T , CM000673.1:g.62622797C>T GRCh37
NC_000011.8:g.62379373C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002564.1:n.42G>A (SNORD26)
NR_003098.1:n.67+99G>A (SNHG1)
NR_003098.2:n.64+99G>A (SNHG1)
NR_152575.1:n.462+99G>A (SNHG1)
NR_152576.1:n.462+99G>A (SNHG1)
NR_152577.1:n.64+99G>A (SNHG1)
NR_152578.1:n.22-109G>A (SNHG1)
NR_152579.1:n.64+99G>A (SNHG1)
NR_152580.1:n.64+99G>A (SNHG1)
NR_152581.1:n.64+99G>A (SNHG1)
NR_152582.1:n.22-109G>A (SNHG1)
NR_152583.1:n.64+99G>A (SNHG1)
NR_152584.1:n.462+99G>A (SNHG1)
NR_152585.1:n.462+99G>A (SNHG1)
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