Canonical Allele Identifier: CA474888867

Gene: SNORD27 SNHG1

Linked Data

• MyVariant Identifiers: chr11:g.62622498A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855026A>C , CM000673.2:g.62855026A>C	GRCh38
NC_000011.9:g.62622498A>C , CM000673.1:g.62622498A>C	GRCh37
NC_000011.8:g.62379074A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002563.1:n.58T>G (SNORD27)
NR_003098.1:n.152-88T>G (SNHG1)
NR_003098.2:n.149-88T>G (SNHG1)
NR_152575.1:n.547-88T>G (SNHG1)
NR_152576.1:n.539-88T>G (SNHG1)
NR_152577.1:n.148+107T>G (SNHG1)
NR_152578.1:n.105+107T>G (SNHG1)
NR_152579.1:n.148+107T>G (SNHG1)
NR_152580.1:n.148+107T>G (SNHG1)
NR_152581.1:n.149-88T>G (SNHG1)
NR_152582.1:n.106-88T>G (SNHG1)
NR_152583.1:n.148+107T>G (SNHG1)
NR_152584.1:n.547-88T>G (SNHG1)
NR_152585.1:n.546+107T>G (SNHG1)