Canonical Allele Identifier: CA474889635

Gene: SNORD26 SNHG1

Linked Data

• MyVariant Identifiers: chr11:g.62622780T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855308T>C , CM000673.2:g.62855308T>C	GRCh38
NC_000011.9:g.62622780T>C , CM000673.1:g.62622780T>C	GRCh37
NC_000011.8:g.62379356T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002564.1:n.59A>G (SNORD26)
NR_003098.1:n.68-92A>G (SNHG1)
NR_003098.2:n.65-92A>G (SNHG1)
NR_152575.1:n.463-92A>G (SNHG1)
NR_152576.1:n.463-100A>G (SNHG1)
NR_152577.1:n.65-92A>G (SNHG1)
NR_152578.1:n.22-92A>G (SNHG1)
NR_152579.1:n.65-92A>G (SNHG1)
NR_152580.1:n.65-92A>G (SNHG1)
NR_152581.1:n.65-92A>G (SNHG1)
NR_152582.1:n.22-92A>G (SNHG1)
NR_152583.1:n.65-92A>G (SNHG1)
NR_152584.1:n.463-92A>G (SNHG1)
NR_152585.1:n.463-92A>G (SNHG1)