Canonical Allele Identifier: CA1977985056

Gene: SNORD26 SNHG1

Linked Data

• dbSNP Id: rs756514499
• gnomAD v4: 11-62855332-AAGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855337_62855340del , CM000673.2:g.62855337_62855340del	GRCh38
NC_000011.9:g.62622809_62622812del , CM000673.1:g.62622809_62622812del	GRCh37
NC_000011.8:g.62379385_62379388del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002564.1:n.31_34del (SNORD26)
NR_003098.1:n.67+88_67+91del (SNHG1)
NR_003098.2:n.64+88_64+91del (SNHG1)
NR_152575.1:n.462+88_462+91del (SNHG1)
NR_152576.1:n.462+88_462+91del (SNHG1)
NR_152577.1:n.64+88_64+91del (SNHG1)
NR_152578.1:n.22-120_22-117del (SNHG1)
NR_152579.1:n.64+88_64+91del (SNHG1)
NR_152580.1:n.64+88_64+91del (SNHG1)
NR_152581.1:n.64+88_64+91del (SNHG1)
NR_152582.1:n.22-120_22-117del (SNHG1)
NR_152583.1:n.64+88_64+91del (SNHG1)
NR_152584.1:n.462+88_462+91del (SNHG1)
NR_152585.1:n.462+88_462+91del (SNHG1)