Canonical Allele Identifier: CA1977985992
Gene: SNORD25 HGNC NCBI
SNHG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855616G= , CM000673.2:g.62855616G= GRCh38
NC_000011.9:g.62623088G= , CM000673.1:g.62623088G= GRCh37
NC_000011.8:g.62379664G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002565.1:n.16C= (SNORD25)
NR_003098.1:n.25-150C= (SNHG1)
NR_003098.2:n.22-150C= (SNHG1)
NR_152575.1:n.270C= (SNHG1)
NR_152576.1:n.270C= (SNHG1)
NR_152577.1:n.22-150C= (SNHG1)
NR_152578.1:n.21+249C= (SNHG1)
NR_152579.1:n.22-150C= (SNHG1)
NR_152580.1:n.22-150C= (SNHG1)
NR_152581.1:n.22-150C= (SNHG1)
NR_152582.1:n.21+249C= (SNHG1)
NR_152583.1:n.22-150C= (SNHG1)
NR_152584.1:n.270C= (SNHG1)
NR_152585.1:n.270C= (SNHG1)