Canonical Allele Identifier: CA6058259
Gene: SNORD25 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs372345167
ExAC: 11:62623065 G / C
gnomAD v2: 11-62623065-G-C
gnomAD v4: 11-62855593-G-C
MyVariant Identifiers: chr11:g.62623065G>C (hg19) chr11:g.62855593G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855593G>C , CM000673.2:g.62855593G>C GRCh38
NC_000011.9:g.62623065G>C , CM000673.1:g.62623065G>C GRCh37
NC_000011.8:g.62379641G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002565.1:n.39C>G (SNORD25)
NR_003098.1:n.25-127C>G (SNHG1)
NR_003098.2:n.22-127C>G (SNHG1)
NR_152575.1:n.293C>G (SNHG1)
NR_152576.1:n.293C>G (SNHG1)
NR_152577.1:n.22-127C>G (SNHG1)
NR_152578.1:n.21+272C>G (SNHG1)
NR_152579.1:n.22-127C>G (SNHG1)
NR_152580.1:n.22-127C>G (SNHG1)
NR_152581.1:n.22-127C>G (SNHG1)
NR_152582.1:n.21+272C>G (SNHG1)
NR_152583.1:n.22-127C>G (SNHG1)
NR_152584.1:n.293C>G (SNHG1)
NR_152585.1:n.293C>G (SNHG1)
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