Canonical Allele Identifier: CA1977985142
Gene: SNORD26 HGNC NCBI
SNHG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855359C= , CM000673.2:g.62855359C= GRCh38
NC_000011.9:g.62622831C= , CM000673.1:g.62622831C= GRCh37
NC_000011.8:g.62379407C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002564.1:n.8G= (SNORD26)
NR_003098.1:n.67+65G= (SNHG1)
NR_003098.2:n.64+65G= (SNHG1)
NR_152575.1:n.462+65G= (SNHG1)
NR_152576.1:n.462+65G= (SNHG1)
NR_152577.1:n.64+65G= (SNHG1)
NR_152578.1:n.22-143G= (SNHG1)
NR_152579.1:n.64+65G= (SNHG1)
NR_152580.1:n.64+65G= (SNHG1)
NR_152581.1:n.64+65G= (SNHG1)
NR_152582.1:n.22-143G= (SNHG1)
NR_152583.1:n.64+65G= (SNHG1)
NR_152584.1:n.462+65G= (SNHG1)
NR_152585.1:n.462+65G= (SNHG1)