Canonical Allele Identifier: CA474889595

Gene: SNORD26 SNHG1

Linked Data

• MyVariant Identifiers: chr11:g.62622765C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855293C>A , CM000673.2:g.62855293C>A	GRCh38
NC_000011.9:g.62622765C>A , CM000673.1:g.62622765C>A	GRCh37
NC_000011.8:g.62379341C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002564.1:n.74G>T (SNORD26)
NR_003098.1:n.68-77G>T (SNHG1)
NR_003098.2:n.65-77G>T (SNHG1)
NR_152575.1:n.463-77G>T (SNHG1)
NR_152576.1:n.463-85G>T (SNHG1)
NR_152577.1:n.65-77G>T (SNHG1)
NR_152578.1:n.22-77G>T (SNHG1)
NR_152579.1:n.65-77G>T (SNHG1)
NR_152580.1:n.65-77G>T (SNHG1)
NR_152581.1:n.65-77G>T (SNHG1)
NR_152582.1:n.22-77G>T (SNHG1)
NR_152583.1:n.65-77G>T (SNHG1)
NR_152584.1:n.463-77G>T (SNHG1)
NR_152585.1:n.463-77G>T (SNHG1)