Canonical Allele Identifier: CA1977983976

Gene: SNORD27 SNHG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855018_62855021delinsCAGT , CM000673.2:g.62855018_62855021delinsCAGT	GRCh38
NC_000011.9:g.62622490_62622493delinsCAGT , CM000673.1:g.62622490_62622493delinsCAGT	GRCh37
NC_000011.8:g.62379066_62379069delinsCAGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002563.1:n.63_66delinsACTG (SNORD27)
NR_003098.1:n.152-83_152-80delinsACTG (SNHG1)
NR_003098.2:n.149-83_149-80delinsACTG (SNHG1)
NR_152575.1:n.547-83_547-80delinsACTG (SNHG1)
NR_152576.1:n.539-83_539-80delinsACTG (SNHG1)
NR_152577.1:n.148+112_148+115delinsACTG (SNHG1)
NR_152578.1:n.105+112_105+115delinsACTG (SNHG1)
NR_152579.1:n.148+112_148+115delinsACTG (SNHG1)
NR_152580.1:n.148+112_148+115delinsACTG (SNHG1)
NR_152581.1:n.149-83_149-80delinsACTG (SNHG1)
NR_152582.1:n.106-83_106-80delinsACTG (SNHG1)
NR_152583.1:n.148+112_148+115delinsACTG (SNHG1)
NR_152584.1:n.547-83_547-80delinsACTG (SNHG1)
NR_152585.1:n.546+112_546+115delinsACTG (SNHG1)