Canonical Allele Identifier: CA474889361
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs2134949424
MyVariant Identifiers: chr11:g.62622677T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855205T>A , CM000673.2:g.62855205T>A GRCh38
NC_000011.9:g.62622677T>A , CM000673.1:g.62622677T>A GRCh37
NC_000011.8:g.62379253T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.79A>T
NR_003098.2:n.76A>T
NR_152575.1:n.474A>T
NR_152576.1:n.466A>T
NR_152577.1:n.76A>T
NR_152578.1:n.33A>T
NR_152579.1:n.76A>T
NR_152580.1:n.76A>T
NR_152581.1:n.76A>T
NR_152582.1:n.33A>T
NR_152583.1:n.76A>T
NR_152584.1:n.474A>T
NR_152585.1:n.474A>T
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