Canonical Allele Identifier: CA1977983963

Gene: SNORD27 SNHG1

Linked Data

• dbSNP Id: rs2085254478

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855015_62855019del , CM000673.2:g.62855015_62855019del	GRCh38
NC_000011.9:g.62622487_62622491del , CM000673.1:g.62622487_62622491del	GRCh37
NC_000011.8:g.62379063_62379067del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002563.1:n.65_69del (SNORD27)
NR_003098.1:n.152-81_152-77del (SNHG1)
NR_003098.2:n.149-81_149-77del (SNHG1)
NR_152575.1:n.547-81_547-77del (SNHG1)
NR_152576.1:n.539-81_539-77del (SNHG1)
NR_152577.1:n.148+114_148+118del (SNHG1)
NR_152578.1:n.105+114_105+118del (SNHG1)
NR_152579.1:n.148+114_148+118del (SNHG1)
NR_152580.1:n.148+114_148+118del (SNHG1)
NR_152581.1:n.149-81_149-77del (SNHG1)
NR_152582.1:n.106-81_106-77del (SNHG1)
NR_152583.1:n.148+114_148+118del (SNHG1)
NR_152584.1:n.547-81_547-77del (SNHG1)
NR_152585.1:n.546+114_546+118del (SNHG1)