Canonical Allele Identifier: CA6058250
Gene: SNORD25 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs746926541

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855574_62855575del , CM000673.2:g.62855574_62855575del GRCh38
NC_000011.9:g.62623046_62623047del , CM000673.1:g.62623046_62623047del GRCh37
NC_000011.8:g.62379622_62379623del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002565.1:n.59_60del (SNORD25)
NR_003098.1:n.25-107_25-106del (SNHG1)
NR_003098.2:n.22-107_22-106del (SNHG1)
NR_152575.1:n.313_314del (SNHG1)
NR_152576.1:n.313_314del (SNHG1)
NR_152577.1:n.22-107_22-106del (SNHG1)
NR_152578.1:n.21+292_21+293del (SNHG1)
NR_152579.1:n.22-107_22-106del (SNHG1)
NR_152580.1:n.22-107_22-106del (SNHG1)
NR_152581.1:n.22-107_22-106del (SNHG1)
NR_152582.1:n.21+292_21+293del (SNHG1)
NR_152583.1:n.22-107_22-106del (SNHG1)
NR_152584.1:n.313_314del (SNHG1)
NR_152585.1:n.313_314del (SNHG1)