Linked Data
gnomAD v4:
18-31598708-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31598708G>A , CM000680.2:g.31598708G>A | GRCh38 |
| NC_000018.9:g.29178671G>A , CM000680.1:g.29178671G>A | GRCh37 |
| NC_000018.8:g.27432669G>A | NCBI36 |
| NG_009490.1:g.11942G>A , LRG_416:g.11942G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237014.8:c.*33G>A MANE Select | ENSP00000237014.4:n.*33G>A | |
| ENST00000610404.5:c.*33G>A | ENSP00000477599.2:n.*33G>A | |
| ENST00000649620.1:c.*33G>A | ENSP00000497927.1:n.*33G>A | |
| ENST00000237014.7:c.*33G>A | ENSP00000237014.3:n.*33G>A | |
| ENST00000610404.4:c.*33G>A | ENSP00000477599.1:n.*33G>A | |
| NM_000371.3:c.*33G>A , LRG_416t1:c.*33G>A | NP_000362.1:n.*33G>A | |
| NM_000371.4:c.*33G>A MANE Select | NP_000362.1:n.*33G>A |