Canonical Allele Identifier: CA474888844

Gene: SNORD27 SNHG1

Linked Data

• MyVariant Identifiers: chr11:g.62622489T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855017T>G , CM000673.2:g.62855017T>G	GRCh38
NC_000011.9:g.62622489T>G , CM000673.1:g.62622489T>G	GRCh37
NC_000011.8:g.62379065T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002563.1:n.67A>C (SNORD27)
NR_003098.1:n.152-79A>C (SNHG1)
NR_003098.2:n.149-79A>C (SNHG1)
NR_152575.1:n.547-79A>C (SNHG1)
NR_152576.1:n.539-79A>C (SNHG1)
NR_152577.1:n.148+116A>C (SNHG1)
NR_152578.1:n.105+116A>C (SNHG1)
NR_152579.1:n.148+116A>C (SNHG1)
NR_152580.1:n.148+116A>C (SNHG1)
NR_152581.1:n.149-79A>C (SNHG1)
NR_152582.1:n.106-79A>C (SNHG1)
NR_152583.1:n.148+116A>C (SNHG1)
NR_152584.1:n.547-79A>C (SNHG1)
NR_152585.1:n.546+116A>C (SNHG1)