Canonical Allele Identifier: CA599798963
Gene: SNORD25 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1565237279

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855569_62855571del , CM000673.2:g.62855569_62855571del GRCh38
NC_000011.9:g.62623041_62623043del , CM000673.1:g.62623041_62623043del GRCh37
NC_000011.8:g.62379617_62379619del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002565.1:n.64_66del (SNORD25)
NR_003098.1:n.25-102_25-100del (SNHG1)
NR_003098.2:n.22-102_22-100del (SNHG1)
NR_152575.1:n.318_320del (SNHG1)
NR_152576.1:n.318_320del (SNHG1)
NR_152577.1:n.22-102_22-100del (SNHG1)
NR_152578.1:n.21+297_21+299del (SNHG1)
NR_152579.1:n.22-102_22-100del (SNHG1)
NR_152580.1:n.22-102_22-100del (SNHG1)
NR_152581.1:n.22-102_22-100del (SNHG1)
NR_152582.1:n.21+297_21+299del (SNHG1)
NR_152583.1:n.22-102_22-100del (SNHG1)
NR_152584.1:n.318_320del (SNHG1)
NR_152585.1:n.318_320del (SNHG1)