Canonical Allele Identifier: CA223667573
Gene: SNORD27 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs992375349
gnomAD v3: 11-62855076-C-G
gnomAD v4: 11-62855076-C-G
MyVariant Identifiers: chr11:g.62622548C>G (hg19) chr11:g.62855076C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855076C>G , CM000673.2:g.62855076C>G GRCh38
NC_000011.9:g.62622548C>G , CM000673.1:g.62622548C>G GRCh37
NC_000011.8:g.62379124C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002563.1:n.8G>C (SNORD27)
NR_003098.1:n.151+57G>C (SNHG1)
NR_003098.2:n.148+57G>C (SNHG1)
NR_152575.1:n.546+57G>C (SNHG1)
NR_152576.1:n.538+57G>C (SNHG1)
NR_152577.1:n.148+57G>C (SNHG1)
NR_152578.1:n.105+57G>C (SNHG1)
NR_152579.1:n.148+57G>C (SNHG1)
NR_152580.1:n.148+57G>C (SNHG1)
NR_152581.1:n.148+57G>C (SNHG1)
NR_152582.1:n.105+57G>C (SNHG1)
NR_152583.1:n.148+57G>C (SNHG1)
NR_152584.1:n.546+57G>C (SNHG1)
NR_152585.1:n.546+57G>C (SNHG1)
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