Canonical Allele Identifier: CA474889807
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1204966325
gnomAD v3: 11-62855372-T-G
gnomAD v4: 11-62855372-T-G
MyVariant Identifiers: chr11:g.62622844T>G (hg19) chr11:g.62855372T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855372T>G , CM000673.2:g.62855372T>G GRCh38
NC_000011.9:g.62622844T>G , CM000673.1:g.62622844T>G GRCh37
NC_000011.8:g.62379420T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.67+52A>C
NR_003098.2:n.64+52A>C
NR_152575.1:n.462+52A>C
NR_152576.1:n.462+52A>C
NR_152577.1:n.64+52A>C
NR_152578.1:n.22-156A>C
NR_152579.1:n.64+52A>C
NR_152580.1:n.64+52A>C
NR_152581.1:n.64+52A>C
NR_152582.1:n.22-156A>C
NR_152583.1:n.64+52A>C
NR_152584.1:n.462+52A>C
NR_152585.1:n.462+52A>C
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