Canonical Allele Identifier: CA599798951

Gene: SNORD26 SNHG1

Linked Data

• dbSNP Id: rs1565236532
• gnomAD v2: 11-62622800-CAG-C
• gnomAD v4: 11-62855328-CAG-C
• MyVariant Identifiers: chr11:g.62622802_62622804delinsA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855330_62855331del , CM000673.2:g.62855330_62855331del	GRCh38
NC_000011.9:g.62622802_62622803del , CM000673.1:g.62622802_62622803del	GRCh37
NC_000011.8:g.62379378_62379379del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002564.1:n.37_38del (SNORD26)
NR_003098.1:n.67+94_67+95del (SNHG1)
NR_003098.2:n.64+94_64+95del (SNHG1)
NR_152575.1:n.462+94_462+95del (SNHG1)
NR_152576.1:n.462+94_462+95del (SNHG1)
NR_152577.1:n.64+94_64+95del (SNHG1)
NR_152578.1:n.22-114_22-113del (SNHG1)
NR_152579.1:n.64+94_64+95del (SNHG1)
NR_152580.1:n.64+94_64+95del (SNHG1)
NR_152581.1:n.64+94_64+95del (SNHG1)
NR_152582.1:n.22-114_22-113del (SNHG1)
NR_152583.1:n.64+94_64+95del (SNHG1)
NR_152584.1:n.462+94_462+95del (SNHG1)
NR_152585.1:n.462+94_462+95del (SNHG1)