Canonical Allele Identifier: CA474890374
Gene: SNORD25 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1428031521
MyVariant Identifiers: chr11:g.62623060A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855588A>G , CM000673.2:g.62855588A>G GRCh38
NC_000011.9:g.62623060A>G , CM000673.1:g.62623060A>G GRCh37
NC_000011.8:g.62379636A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002565.1:n.44T>C (SNORD25)
NR_003098.1:n.25-122T>C (SNHG1)
NR_003098.2:n.22-122T>C (SNHG1)
NR_152575.1:n.298T>C (SNHG1)
NR_152576.1:n.298T>C (SNHG1)
NR_152577.1:n.22-122T>C (SNHG1)
NR_152578.1:n.21+277T>C (SNHG1)
NR_152579.1:n.22-122T>C (SNHG1)
NR_152580.1:n.22-122T>C (SNHG1)
NR_152581.1:n.22-122T>C (SNHG1)
NR_152582.1:n.21+277T>C (SNHG1)
NR_152583.1:n.22-122T>C (SNHG1)
NR_152584.1:n.298T>C (SNHG1)
NR_152585.1:n.298T>C (SNHG1)