Canonical Allele Identifier: CA2741179158
Gene: SNORD27 HGNC NCBI
SNHG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855047_62855066del , CM000673.2:g.62855047_62855066del GRCh38
NC_000011.9:g.62622519_62622538del , CM000673.1:g.62622519_62622538del GRCh37
NC_000011.8:g.62379095_62379114del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002563.1:n.20_39del (SNORD27)
NR_003098.1:n.151+69_151+88del (SNHG1)
NR_003098.2:n.148+69_148+88del (SNHG1)
NR_152575.1:n.546+69_546+88del (SNHG1)
NR_152576.1:n.538+69_538+88del (SNHG1)
NR_152577.1:n.148+69_148+88del (SNHG1)
NR_152578.1:n.105+69_105+88del (SNHG1)
NR_152579.1:n.148+69_148+88del (SNHG1)
NR_152580.1:n.148+69_148+88del (SNHG1)
NR_152581.1:n.148+69_148+88del (SNHG1)
NR_152582.1:n.105+69_105+88del (SNHG1)
NR_152583.1:n.148+69_148+88del (SNHG1)
NR_152584.1:n.546+69_546+88del (SNHG1)
NR_152585.1:n.546+69_546+88del (SNHG1)
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