Canonical Allele Identifier: CA6058253
Gene: SNORD25 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1059292

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855579T>C , CM000673.2:g.62855579T>C GRCh38
NC_000011.9:g.62623051T>C , CM000673.1:g.62623051T>C GRCh37
NC_000011.8:g.62379627T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002565.1:n.53A>G (SNORD25)
NR_003098.1:n.25-113A>G (SNHG1)
NR_003098.2:n.22-113A>G (SNHG1)
NR_152575.1:n.307A>G (SNHG1)
NR_152576.1:n.307A>G (SNHG1)
NR_152577.1:n.22-113A>G (SNHG1)
NR_152578.1:n.21+286A>G (SNHG1)
NR_152579.1:n.22-113A>G (SNHG1)
NR_152580.1:n.22-113A>G (SNHG1)
NR_152581.1:n.22-113A>G (SNHG1)
NR_152582.1:n.21+286A>G (SNHG1)
NR_152583.1:n.22-113A>G (SNHG1)
NR_152584.1:n.307A>G (SNHG1)
NR_152585.1:n.307A>G (SNHG1)