Canonical Allele Identifier: CA6058128
Gene: SNORD27 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs766980197
ExAC: 11:62622508 A / C
gnomAD v2: 11-62622508-A-C
gnomAD v4: 11-62855036-A-C
MyVariant Identifiers: chr11:g.62622508A>C (hg19) chr11:g.62855036A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855036A>C , CM000673.2:g.62855036A>C GRCh38
NC_000011.9:g.62622508A>C , CM000673.1:g.62622508A>C GRCh37
NC_000011.8:g.62379084A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002563.1:n.48T>G (SNORD27)
NR_003098.1:n.152-98T>G (SNHG1)
NR_003098.2:n.149-98T>G (SNHG1)
NR_152575.1:n.547-98T>G (SNHG1)
NR_152576.1:n.539-98T>G (SNHG1)
NR_152577.1:n.148+97T>G (SNHG1)
NR_152578.1:n.105+97T>G (SNHG1)
NR_152579.1:n.148+97T>G (SNHG1)
NR_152580.1:n.148+97T>G (SNHG1)
NR_152581.1:n.149-98T>G (SNHG1)
NR_152582.1:n.106-98T>G (SNHG1)
NR_152583.1:n.148+97T>G (SNHG1)
NR_152584.1:n.547-98T>G (SNHG1)
NR_152585.1:n.546+97T>G (SNHG1)
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