Canonical Allele Identifier: CA1977985897
Gene: SNORD25 HGNC NCBI
SNHG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855594C= , CM000673.2:g.62855594C= GRCh38
NC_000011.9:g.62623066C= , CM000673.1:g.62623066C= GRCh37
NC_000011.8:g.62379642C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002565.1:n.38G= (SNORD25)
NR_003098.1:n.25-128G= (SNHG1)
NR_003098.2:n.22-128G= (SNHG1)
NR_152575.1:n.292G= (SNHG1)
NR_152576.1:n.292G= (SNHG1)
NR_152577.1:n.22-128G= (SNHG1)
NR_152578.1:n.21+271G= (SNHG1)
NR_152579.1:n.22-128G= (SNHG1)
NR_152580.1:n.22-128G= (SNHG1)
NR_152581.1:n.22-128G= (SNHG1)
NR_152582.1:n.21+271G= (SNHG1)
NR_152583.1:n.22-128G= (SNHG1)
NR_152584.1:n.292G= (SNHG1)
NR_152585.1:n.292G= (SNHG1)