Canonical Allele Identifier: CA474889010
Gene: SNORD27 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1317106641
gnomAD v2: 11-62622552-G-T
gnomAD v4: 11-62855080-G-T
MyVariant Identifiers: chr11:g.62622552G>T (hg19) chr11:g.62855080G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855080G>T , CM000673.2:g.62855080G>T GRCh38
NC_000011.9:g.62622552G>T , CM000673.1:g.62622552G>T GRCh37
NC_000011.8:g.62379128G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002563.1:n.4C>A (SNORD27)
NR_003098.1:n.151+53C>A (SNHG1)
NR_003098.2:n.148+53C>A (SNHG1)
NR_152575.1:n.546+53C>A (SNHG1)
NR_152576.1:n.538+53C>A (SNHG1)
NR_152577.1:n.148+53C>A (SNHG1)
NR_152578.1:n.105+53C>A (SNHG1)
NR_152579.1:n.148+53C>A (SNHG1)
NR_152580.1:n.148+53C>A (SNHG1)
NR_152581.1:n.148+53C>A (SNHG1)
NR_152582.1:n.105+53C>A (SNHG1)
NR_152583.1:n.148+53C>A (SNHG1)
NR_152584.1:n.546+53C>A (SNHG1)
NR_152585.1:n.546+53C>A (SNHG1)
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