Canonical Allele Identifier: CA599798948
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1408094295
gnomAD v2: 11-62622570-TCTC-T
gnomAD v3: 11-62855098-TCTC-T
gnomAD v4: 11-62855098-TCTC-T
MyVariant Identifiers: chr11:g.62622571_62622573del (hg19) chr11:g.62855099_62855101del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855102_62855104del , CM000673.2:g.62855102_62855104del GRCh38
NC_000011.9:g.62622574_62622576del , CM000673.1:g.62622574_62622576del GRCh37
NC_000011.8:g.62379150_62379152del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.151+32_151+34del
NR_003098.2:n.148+32_148+34del
NR_152575.1:n.546+32_546+34del
NR_152576.1:n.538+32_538+34del
NR_152577.1:n.148+32_148+34del
NR_152578.1:n.105+32_105+34del
NR_152579.1:n.148+32_148+34del
NR_152580.1:n.148+32_148+34del
NR_152581.1:n.148+32_148+34del
NR_152582.1:n.105+32_105+34del
NR_152583.1:n.148+32_148+34del
NR_152584.1:n.546+32_546+34del
NR_152585.1:n.546+32_546+34del
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