Canonical Allele Identifier: CA1977985050
Gene: SNORD26 HGNC NCBI
SNHG1 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_002564.1:n.37C= (SNORD26)
NR_003098.1:n.67+94C= (SNHG1)
NR_003098.2:n.64+94C= (SNHG1)
NR_152575.1:n.462+94C= (SNHG1)
NR_152576.1:n.462+94C= (SNHG1)
NR_152577.1:n.64+94C= (SNHG1)
NR_152578.1:n.22-114C= (SNHG1)
NR_152579.1:n.64+94C= (SNHG1)
NR_152580.1:n.64+94C= (SNHG1)
NR_152581.1:n.64+94C= (SNHG1)
NR_152582.1:n.22-114C= (SNHG1)
NR_152583.1:n.64+94C= (SNHG1)
NR_152584.1:n.462+94C= (SNHG1)
NR_152585.1:n.462+94C= (SNHG1)
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