Canonical Allele Identifier: CA1977986020

Gene: SNORD25 SNHG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855619_62855622delinsCTCA , CM000673.2:g.62855619_62855622delinsCTCA	GRCh38
NC_000011.9:g.62623091_62623094delinsCTCA , CM000673.1:g.62623091_62623094delinsCTCA	GRCh37
NC_000011.8:g.62379667_62379670delinsCTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002565.1:n.10_13delinsTGAG (SNORD25)
NR_003098.1:n.25-156_25-153delinsTGAG (SNHG1)
NR_003098.2:n.22-156_22-153delinsTGAG (SNHG1)
NR_152575.1:n.264_267delinsTGAG (SNHG1)
NR_152576.1:n.264_267delinsTGAG (SNHG1)
NR_152577.1:n.22-156_22-153delinsTGAG (SNHG1)
NR_152578.1:n.21+243_21+246delinsTGAG (SNHG1)
NR_152579.1:n.22-156_22-153delinsTGAG (SNHG1)
NR_152580.1:n.22-156_22-153delinsTGAG (SNHG1)
NR_152581.1:n.22-156_22-153delinsTGAG (SNHG1)
NR_152582.1:n.21+243_21+246delinsTGAG (SNHG1)
NR_152583.1:n.22-156_22-153delinsTGAG (SNHG1)
NR_152584.1:n.264_267delinsTGAG (SNHG1)
NR_152585.1:n.264_267delinsTGAG (SNHG1)