Canonical Allele Identifier: CA474889607
Gene: SNORD26 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.62622769T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855297T>A , CM000673.2:g.62855297T>A GRCh38
NC_000011.9:g.62622769T>A , CM000673.1:g.62622769T>A GRCh37
NC_000011.8:g.62379345T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002564.1:n.70A>T (SNORD26)
NR_003098.1:n.68-81A>T (SNHG1)
NR_003098.2:n.65-81A>T (SNHG1)
NR_152575.1:n.463-81A>T (SNHG1)
NR_152576.1:n.463-89A>T (SNHG1)
NR_152577.1:n.65-81A>T (SNHG1)
NR_152578.1:n.22-81A>T (SNHG1)
NR_152579.1:n.65-81A>T (SNHG1)
NR_152580.1:n.65-81A>T (SNHG1)
NR_152581.1:n.65-81A>T (SNHG1)
NR_152582.1:n.22-81A>T (SNHG1)
NR_152583.1:n.65-81A>T (SNHG1)
NR_152584.1:n.463-81A>T (SNHG1)
NR_152585.1:n.463-81A>T (SNHG1)