Canonical Allele Identifier: CA6058162
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs766276867
ExAC: 11:62622716 C / T
gnomAD v2: 11-62622716-C-T
gnomAD v4: 11-62855244-C-T
MyVariant Identifiers: chr11:g.62622716C>T (hg19) chr11:g.62855244C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855244C>T , CM000673.2:g.62855244C>T GRCh38
NC_000011.9:g.62622716C>T , CM000673.1:g.62622716C>T GRCh37
NC_000011.8:g.62379292C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.68-28G>A
NR_003098.2:n.65-28G>A
NR_152575.1:n.463-28G>A
NR_152576.1:n.463-36G>A
NR_152577.1:n.65-28G>A
NR_152578.1:n.22-28G>A
NR_152579.1:n.65-28G>A
NR_152580.1:n.65-28G>A
NR_152581.1:n.65-28G>A
NR_152582.1:n.22-28G>A
NR_152583.1:n.65-28G>A
NR_152584.1:n.463-28G>A
NR_152585.1:n.463-28G>A
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