Linked Data
gnomAD v4:
11-130403439-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.130403439C>T , CM000673.2:g.130403439C>T | GRCh38 |
| NC_000011.9:g.130273334C>T , CM000673.1:g.130273334C>T | GRCh37 |
| NC_000011.8:g.129778544C>T | NCBI36 |
| NG_052870.1:g.30555G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948177.1:n.2534C>T | ||
| XR_948178.1:n.2188C>T | ||
| XR_948179.1:n.2106C>T | ||
| XR_948180.1:n.2106C>T | ||
| XR_948181.1:n.675C>T | ||
| XR_948182.1:n.2266C>T | ||
| XR_948183.1:n.458+9640C>T | ||
| XR_948184.1:n.597C>T | ||
| XR_948185.1:n.526C>T | ||
| XR_948187.1:n.458+9640C>T | ||
| XR_948188.1:n.429C>T | ||
| XR_948189.1:n.477C>T | ||
| NR_148980.1:n.750C>T |