Canonical Allele Identifier: CA6058261

Gene: SNORD25 SNHG1

Linked Data

• dbSNP Id: rs555147172
• ExAC: 11:62623071 T / C
• gnomAD v2: 11-62623071-T-C
• gnomAD v4: 11-62855599-T-C
• MyVariant Identifiers: chr11:g.62623071T>C (hg19) ; chr11:g.62855599T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855599T>C , CM000673.2:g.62855599T>C	GRCh38
NC_000011.9:g.62623071T>C , CM000673.1:g.62623071T>C	GRCh37
NC_000011.8:g.62379647T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002565.1:n.33A>G (SNORD25)
NR_003098.1:n.25-133A>G (SNHG1)
NR_003098.2:n.22-133A>G (SNHG1)
NR_152575.1:n.287A>G (SNHG1)
NR_152576.1:n.287A>G (SNHG1)
NR_152577.1:n.22-133A>G (SNHG1)
NR_152578.1:n.21+266A>G (SNHG1)
NR_152579.1:n.22-133A>G (SNHG1)
NR_152580.1:n.22-133A>G (SNHG1)
NR_152581.1:n.22-133A>G (SNHG1)
NR_152582.1:n.21+266A>G (SNHG1)
NR_152583.1:n.22-133A>G (SNHG1)
NR_152584.1:n.287A>G (SNHG1)
NR_152585.1:n.287A>G (SNHG1)