Linked Data
gnomAD v4:
11-130403465-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.130403465C>T , CM000673.2:g.130403465C>T | GRCh38 |
| NC_000011.9:g.130273360C>T , CM000673.1:g.130273360C>T | GRCh37 |
| NC_000011.8:g.129778570C>T | NCBI36 |
| NG_052870.1:g.30529G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948177.1:n.2560C>T | ||
| XR_948178.1:n.2214C>T | ||
| XR_948179.1:n.2132C>T | ||
| XR_948180.1:n.2132C>T | ||
| XR_948181.1:n.701C>T | ||
| XR_948182.1:n.2292C>T | ||
| XR_948183.1:n.458+9666C>T | ||
| XR_948184.1:n.623C>T | ||
| XR_948185.1:n.552C>T | ||
| XR_948187.1:n.458+9666C>T | ||
| XR_948188.1:n.455C>T | ||
| XR_948189.1:n.503C>T | ||
| NR_148980.1:n.776C>T |