Canonical Allele Identifier: CA474890418
Gene: SNORD25 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.62623078C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855606C>T , CM000673.2:g.62855606C>T GRCh38
NC_000011.9:g.62623078C>T , CM000673.1:g.62623078C>T GRCh37
NC_000011.8:g.62379654C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002565.1:n.26G>A (SNORD25)
NR_003098.1:n.25-140G>A (SNHG1)
NR_003098.2:n.22-140G>A (SNHG1)
NR_152575.1:n.280G>A (SNHG1)
NR_152576.1:n.280G>A (SNHG1)
NR_152577.1:n.22-140G>A (SNHG1)
NR_152578.1:n.21+259G>A (SNHG1)
NR_152579.1:n.22-140G>A (SNHG1)
NR_152580.1:n.22-140G>A (SNHG1)
NR_152581.1:n.22-140G>A (SNHG1)
NR_152582.1:n.21+259G>A (SNHG1)
NR_152583.1:n.22-140G>A (SNHG1)
NR_152584.1:n.280G>A (SNHG1)
NR_152585.1:n.280G>A (SNHG1)