Linked Data
gnomAD v4:
11-130403457-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.130403457G>T , CM000673.2:g.130403457G>T | GRCh38 |
| NC_000011.9:g.130273352G>T , CM000673.1:g.130273352G>T | GRCh37 |
| NC_000011.8:g.129778562G>T | NCBI36 |
| NG_052870.1:g.30537C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948177.1:n.2552G>T | ||
| XR_948178.1:n.2206G>T | ||
| XR_948179.1:n.2124G>T | ||
| XR_948180.1:n.2124G>T | ||
| XR_948181.1:n.693G>T | ||
| XR_948182.1:n.2284G>T | ||
| XR_948183.1:n.458+9658G>T | ||
| XR_948184.1:n.615G>T | ||
| XR_948185.1:n.544G>T | ||
| XR_948187.1:n.458+9658G>T | ||
| XR_948188.1:n.447G>T | ||
| XR_948189.1:n.495G>T | ||
| NR_148980.1:n.768G>T |