Linked Data
gnomAD v4:
11-130403364-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.130403364T>G , CM000673.2:g.130403364T>G | GRCh38 |
| NC_000011.9:g.130273259T>G , CM000673.1:g.130273259T>G | GRCh37 |
| NC_000011.8:g.129778469T>G | NCBI36 |
| NG_052870.1:g.30630A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948177.1:n.2459T>G | ||
| XR_948178.1:n.2113T>G | ||
| XR_948179.1:n.2031T>G | ||
| XR_948180.1:n.2031T>G | ||
| XR_948181.1:n.600T>G | ||
| XR_948182.1:n.2191T>G | ||
| XR_948183.1:n.458+9565T>G | ||
| XR_948184.1:n.522T>G | ||
| XR_948185.1:n.451T>G | ||
| XR_948187.1:n.458+9565T>G | ||
| XR_948188.1:n.354T>G | ||
| XR_948189.1:n.402T>G | ||
| NR_148980.1:n.675T>G |