Canonical Allele Identifier: CA679077591
Gene: SNORD25 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1192324266
gnomAD v3: 11-62855586-TC-T
gnomAD v4: 11-62855586-TC-T
MyVariant Identifiers: chr11:g.62623059del (hg19) chr11:g.62855587del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855587del , CM000673.2:g.62855587del GRCh38
NC_000011.9:g.62623059del , CM000673.1:g.62623059del GRCh37
NC_000011.8:g.62379635del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002565.1:n.45del (SNORD25)
NR_003098.1:n.25-121del (SNHG1)
NR_003098.2:n.22-121del (SNHG1)
NR_152575.1:n.299del (SNHG1)
NR_152576.1:n.299del (SNHG1)
NR_152577.1:n.22-121del (SNHG1)
NR_152578.1:n.21+278del (SNHG1)
NR_152579.1:n.22-121del (SNHG1)
NR_152580.1:n.22-121del (SNHG1)
NR_152581.1:n.22-121del (SNHG1)
NR_152582.1:n.21+278del (SNHG1)
NR_152583.1:n.22-121del (SNHG1)
NR_152584.1:n.299del (SNHG1)
NR_152585.1:n.299del (SNHG1)
Search 100 bp 5'
Search 100 bp 3'