Canonical Allele Identifier: CA599798946
Gene: SNORD27 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1389959618
gnomAD v2: 11-62622520-AGCCATAT-A
gnomAD v4: 11-62855048-AGCCATAT-A
MyVariant Identifiers: chr11:g.62622521_62622527del (hg19) chr11:g.62855049_62855055del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855051_62855057del , CM000673.2:g.62855051_62855057del GRCh38
NC_000011.9:g.62622523_62622529del , CM000673.1:g.62622523_62622529del GRCh37
NC_000011.8:g.62379099_62379105del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002563.1:n.29_35del (SNORD27)
NR_003098.1:n.151+78_151+84del (SNHG1)
NR_003098.2:n.148+78_148+84del (SNHG1)
NR_152575.1:n.546+78_546+84del (SNHG1)
NR_152576.1:n.538+78_538+84del (SNHG1)
NR_152577.1:n.148+78_148+84del (SNHG1)
NR_152578.1:n.105+78_105+84del (SNHG1)
NR_152579.1:n.148+78_148+84del (SNHG1)
NR_152580.1:n.148+78_148+84del (SNHG1)
NR_152581.1:n.148+78_148+84del (SNHG1)
NR_152582.1:n.105+78_105+84del (SNHG1)
NR_152583.1:n.148+78_148+84del (SNHG1)
NR_152584.1:n.546+78_546+84del (SNHG1)
NR_152585.1:n.546+78_546+84del (SNHG1)
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