Canonical Allele Identifier: CA474888870

Gene: SNORD27 SNHG1

Linked Data

• dbSNP Id: rs1293959540
• gnomAD v2: 11-62622499-G-A
• gnomAD v4: 11-62855027-G-A
• MyVariant Identifiers: chr11:g.62622499G>A (hg19) ; chr11:g.62855027G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855027G>A , CM000673.2:g.62855027G>A	GRCh38
NC_000011.9:g.62622499G>A , CM000673.1:g.62622499G>A	GRCh37
NC_000011.8:g.62379075G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002563.1:n.57C>T (SNORD27)
NR_003098.1:n.152-89C>T (SNHG1)
NR_003098.2:n.149-89C>T (SNHG1)
NR_152575.1:n.547-89C>T (SNHG1)
NR_152576.1:n.539-89C>T (SNHG1)
NR_152577.1:n.148+106C>T (SNHG1)
NR_152578.1:n.105+106C>T (SNHG1)
NR_152579.1:n.148+106C>T (SNHG1)
NR_152580.1:n.148+106C>T (SNHG1)
NR_152581.1:n.149-89C>T (SNHG1)
NR_152582.1:n.106-89C>T (SNHG1)
NR_152583.1:n.148+106C>T (SNHG1)
NR_152584.1:n.547-89C>T (SNHG1)
NR_152585.1:n.546+106C>T (SNHG1)