Canonical Allele Identifier: CA1977984260
Gene: SNORD27 HGNC NCBI
SNHG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855080G= , CM000673.2:g.62855080G= GRCh38
NC_000011.9:g.62622552G= , CM000673.1:g.62622552G= GRCh37
NC_000011.8:g.62379128G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002563.1:n.4C= (SNORD27)
NR_003098.1:n.151+53C= (SNHG1)
NR_003098.2:n.148+53C= (SNHG1)
NR_152575.1:n.546+53C= (SNHG1)
NR_152576.1:n.538+53C= (SNHG1)
NR_152577.1:n.148+53C= (SNHG1)
NR_152578.1:n.105+53C= (SNHG1)
NR_152579.1:n.148+53C= (SNHG1)
NR_152580.1:n.148+53C= (SNHG1)
NR_152581.1:n.148+53C= (SNHG1)
NR_152582.1:n.105+53C= (SNHG1)
NR_152583.1:n.148+53C= (SNHG1)
NR_152584.1:n.546+53C= (SNHG1)
NR_152585.1:n.546+53C= (SNHG1)