Canonical Allele Identifier: CA474889719
Gene: SNORD26 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs2085272033
MyVariant Identifiers: chr11:g.62622812G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855340G>C , CM000673.2:g.62855340G>C GRCh38
NC_000011.9:g.62622812G>C , CM000673.1:g.62622812G>C GRCh37
NC_000011.8:g.62379388G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002564.1:n.27C>G (SNORD26)
NR_003098.1:n.67+84C>G (SNHG1)
NR_003098.2:n.64+84C>G (SNHG1)
NR_152575.1:n.462+84C>G (SNHG1)
NR_152576.1:n.462+84C>G (SNHG1)
NR_152577.1:n.64+84C>G (SNHG1)
NR_152578.1:n.22-124C>G (SNHG1)
NR_152579.1:n.64+84C>G (SNHG1)
NR_152580.1:n.64+84C>G (SNHG1)
NR_152581.1:n.64+84C>G (SNHG1)
NR_152582.1:n.22-124C>G (SNHG1)
NR_152583.1:n.64+84C>G (SNHG1)
NR_152584.1:n.462+84C>G (SNHG1)
NR_152585.1:n.462+84C>G (SNHG1)