Canonical Allele Identifier: CA223668506
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs893933546
gnomAD v3: 11-62855780-T-C
gnomAD v4: 11-62855780-T-C
MyVariant Identifiers: chr11:g.62623252T>C (hg19) chr11:g.62855780T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855780T>C , CM000673.2:g.62855780T>C GRCh38
NC_000011.9:g.62623252T>C , CM000673.1:g.62623252T>C GRCh37
NC_000011.8:g.62379828T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.24+85A>G
NR_003098.2:n.21+85A>G
NR_152575.1:n.106A>G
NR_152576.1:n.106A>G
NR_152577.1:n.21+85A>G
NR_152578.1:n.21+85A>G
NR_152579.1:n.21+85A>G
NR_152580.1:n.21+85A>G
NR_152581.1:n.21+85A>G
NR_152582.1:n.21+85A>G
NR_152583.1:n.21+85A>G
NR_152584.1:n.106A>G
NR_152585.1:n.106A>G
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