Canonical Allele Identifier: CA474888841

Gene: SNORD27 SNHG1

Linked Data

• dbSNP Id: rs749443669
• MyVariant Identifiers: chr11:g.62622488C>G (hg19) ; chr11:g.62855016C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855016C>G , CM000673.2:g.62855016C>G	GRCh38
NC_000011.9:g.62622488C>G , CM000673.1:g.62622488C>G	GRCh37
NC_000011.8:g.62379064C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002563.1:n.68G>C (SNORD27)
NR_003098.1:n.152-78G>C (SNHG1)
NR_003098.2:n.149-78G>C (SNHG1)
NR_152575.1:n.547-78G>C (SNHG1)
NR_152576.1:n.539-78G>C (SNHG1)
NR_152577.1:n.148+117G>C (SNHG1)
NR_152578.1:n.105+117G>C (SNHG1)
NR_152579.1:n.148+117G>C (SNHG1)
NR_152580.1:n.148+117G>C (SNHG1)
NR_152581.1:n.149-78G>C (SNHG1)
NR_152582.1:n.106-78G>C (SNHG1)
NR_152583.1:n.148+117G>C (SNHG1)
NR_152584.1:n.547-78G>C (SNHG1)
NR_152585.1:n.546+117G>C (SNHG1)