Canonical Allele Identifier: CA6058201
Gene: SNORD26 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs770130546
ExAC: 11:62622821 G / A
gnomAD v2: 11-62622821-G-A
gnomAD v4: 11-62855349-G-A
MyVariant Identifiers: chr11:g.62622821G>A (hg19) chr11:g.62855349G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855349G>A , CM000673.2:g.62855349G>A GRCh38
NC_000011.9:g.62622821G>A , CM000673.1:g.62622821G>A GRCh37
NC_000011.8:g.62379397G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002564.1:n.18C>T (SNORD26)
NR_003098.1:n.67+75C>T (SNHG1)
NR_003098.2:n.64+75C>T (SNHG1)
NR_152575.1:n.462+75C>T (SNHG1)
NR_152576.1:n.462+75C>T (SNHG1)
NR_152577.1:n.64+75C>T (SNHG1)
NR_152578.1:n.22-133C>T (SNHG1)
NR_152579.1:n.64+75C>T (SNHG1)
NR_152580.1:n.64+75C>T (SNHG1)
NR_152581.1:n.64+75C>T (SNHG1)
NR_152582.1:n.22-133C>T (SNHG1)
NR_152583.1:n.64+75C>T (SNHG1)
NR_152584.1:n.462+75C>T (SNHG1)
NR_152585.1:n.462+75C>T (SNHG1)
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