Linked Data
MyVariant Identifiers:
chr11:g.62622827T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.62855355T>G , CM000673.2:g.62855355T>G | GRCh38 |
| NC_000011.9:g.62622827T>G , CM000673.1:g.62622827T>G | GRCh37 |
| NC_000011.8:g.62379403T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_002564.1:n.12A>C (SNORD26) | ||
| NR_003098.1:n.67+69A>C (SNHG1) | ||
| NR_003098.2:n.64+69A>C (SNHG1) | ||
| NR_152575.1:n.462+69A>C (SNHG1) | ||
| NR_152576.1:n.462+69A>C (SNHG1) | ||
| NR_152577.1:n.64+69A>C (SNHG1) | ||
| NR_152578.1:n.22-139A>C (SNHG1) | ||
| NR_152579.1:n.64+69A>C (SNHG1) | ||
| NR_152580.1:n.64+69A>C (SNHG1) | ||
| NR_152581.1:n.64+69A>C (SNHG1) | ||
| NR_152582.1:n.22-139A>C (SNHG1) | ||
| NR_152583.1:n.64+69A>C (SNHG1) | ||
| NR_152584.1:n.462+69A>C (SNHG1) | ||
| NR_152585.1:n.462+69A>C (SNHG1) |