Canonical Allele Identifier: CA599798950

Gene: SNORD26 SNHG1

Linked Data

• dbSNP Id: rs1177344799
• gnomAD v2: 11-62622764-GCTA-G
• gnomAD v4: 11-62855292-GCTA-G
• MyVariant Identifiers: chr11:g.62622765_62622767del (hg19) ; chr11:g.62855293_62855295del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855295_62855297del , CM000673.2:g.62855295_62855297del	GRCh38
NC_000011.9:g.62622767_62622769del , CM000673.1:g.62622767_62622769del	GRCh37
NC_000011.8:g.62379343_62379345del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002564.1:n.72_74del (SNORD26)
NR_003098.1:n.68-79_68-77del (SNHG1)
NR_003098.2:n.65-79_65-77del (SNHG1)
NR_152575.1:n.463-79_463-77del (SNHG1)
NR_152576.1:n.463-87_463-85del (SNHG1)
NR_152577.1:n.65-79_65-77del (SNHG1)
NR_152578.1:n.22-79_22-77del (SNHG1)
NR_152579.1:n.65-79_65-77del (SNHG1)
NR_152580.1:n.65-79_65-77del (SNHG1)
NR_152581.1:n.65-79_65-77del (SNHG1)
NR_152582.1:n.22-79_22-77del (SNHG1)
NR_152583.1:n.65-79_65-77del (SNHG1)
NR_152584.1:n.463-79_463-77del (SNHG1)
NR_152585.1:n.463-79_463-77del (SNHG1)