Canonical Allele Identifier: CA474890856
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs940655961
gnomAD v2: 11-62623245-T-C
gnomAD v3: 11-62855773-T-C
gnomAD v4: 11-62855773-T-C
MyVariant Identifiers: chr11:g.62623245T>C (hg19) chr11:g.62855773T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855773T>C , CM000673.2:g.62855773T>C GRCh38
NC_000011.9:g.62623245T>C , CM000673.1:g.62623245T>C GRCh37
NC_000011.8:g.62379821T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.24+92A>G
NR_003098.2:n.21+92A>G
NR_152575.1:n.113A>G
NR_152576.1:n.113A>G
NR_152577.1:n.21+92A>G
NR_152578.1:n.21+92A>G
NR_152579.1:n.21+92A>G
NR_152580.1:n.21+92A>G
NR_152581.1:n.21+92A>G
NR_152582.1:n.21+92A>G
NR_152583.1:n.21+92A>G
NR_152584.1:n.113A>G
NR_152585.1:n.113A>G
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