Linked Data
dbSNP Id:
rs1045171039
gnomAD v2:
11-62623100-G-A
gnomAD v3:
11-62855628-G-A
gnomAD v4:
11-62855628-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.62855628G>A , CM000673.2:g.62855628G>A | GRCh38 |
| NC_000011.9:g.62623100G>A , CM000673.1:g.62623100G>A | GRCh37 |
| NC_000011.8:g.62379676G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_002565.1:n.4C>T (SNORD25) | ||
| NR_003098.1:n.25-162C>T (SNHG1) | ||
| NR_003098.2:n.22-162C>T (SNHG1) | ||
| NR_152575.1:n.258C>T (SNHG1) | ||
| NR_152576.1:n.258C>T (SNHG1) | ||
| NR_152577.1:n.22-162C>T (SNHG1) | ||
| NR_152578.1:n.21+237C>T (SNHG1) | ||
| NR_152579.1:n.22-162C>T (SNHG1) | ||
| NR_152580.1:n.22-162C>T (SNHG1) | ||
| NR_152581.1:n.22-162C>T (SNHG1) | ||
| NR_152582.1:n.21+237C>T (SNHG1) | ||
| NR_152583.1:n.22-162C>T (SNHG1) | ||
| NR_152584.1:n.258C>T (SNHG1) | ||
| NR_152585.1:n.258C>T (SNHG1) |