Canonical Allele Identifier: CA938716108

Gene: SNORD27 SNHG1

Linked Data

• dbSNP Id: rs2085254693
• gnomAD v3: 11-62855017-TCAGTAGTAAGATGACATCACTTGAAAGTTCAGCCATA-T
• gnomAD v4: 11-62855017-TCAGTAGTAAGATGACATCACTTGAAAGTTCAGCCATA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855018_62855054del , CM000673.2:g.62855018_62855054del	GRCh38
NC_000011.9:g.62622490_62622526del , CM000673.1:g.62622490_62622526del	GRCh37
NC_000011.8:g.62379066_62379102del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002563.1:n.30_66del (SNORD27)
NR_003098.1:n.151+79_152-80del (SNHG1)
NR_003098.2:n.148+79_149-80del (SNHG1)
NR_152575.1:n.546+79_547-80del (SNHG1)
NR_152576.1:n.538+79_539-80del (SNHG1)
NR_152577.1:n.148+79_148+115del (SNHG1)
NR_152578.1:n.105+79_105+115del (SNHG1)
NR_152579.1:n.148+79_148+115del (SNHG1)
NR_152580.1:n.148+79_148+115del (SNHG1)
NR_152581.1:n.148+79_149-80del (SNHG1)
NR_152582.1:n.105+79_106-80del (SNHG1)
NR_152583.1:n.148+79_148+115del (SNHG1)
NR_152584.1:n.546+79_547-80del (SNHG1)
NR_152585.1:n.546+79_546+115del (SNHG1)