Canonical Allele Identifier: CA6058194

Gene: SNORD26 SNHG1

Linked Data

• dbSNP Id: rs777746559
• ExAC: 11:62622802 G / C
• gnomAD v2: 11-62622802-G-C
• gnomAD v4: 11-62855330-G-C
• MyVariant Identifiers: chr11:g.62622802G>C (hg19) ; chr11:g.62855330G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855330G>C , CM000673.2:g.62855330G>C	GRCh38
NC_000011.9:g.62622802G>C , CM000673.1:g.62622802G>C	GRCh37
NC_000011.8:g.62379378G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002564.1:n.37C>G (SNORD26)
NR_003098.1:n.67+94C>G (SNHG1)
NR_003098.2:n.64+94C>G (SNHG1)
NR_152575.1:n.462+94C>G (SNHG1)
NR_152576.1:n.462+94C>G (SNHG1)
NR_152577.1:n.64+94C>G (SNHG1)
NR_152578.1:n.22-114C>G (SNHG1)
NR_152579.1:n.64+94C>G (SNHG1)
NR_152580.1:n.64+94C>G (SNHG1)
NR_152581.1:n.64+94C>G (SNHG1)
NR_152582.1:n.22-114C>G (SNHG1)
NR_152583.1:n.64+94C>G (SNHG1)
NR_152584.1:n.462+94C>G (SNHG1)
NR_152585.1:n.462+94C>G (SNHG1)