Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31598696C>A , CM000680.2:g.31598696C>A | GRCh38 |
| NC_000018.9:g.29178659C>A , CM000680.1:g.29178659C>A | GRCh37 |
| NC_000018.8:g.27432657C>A | NCBI36 |
| NG_009490.1:g.11930C>A , LRG_416:g.11930C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237014.8:c.*21C>A MANE Select | ENSP00000237014.4:n.*21C>A | |
| ENST00000610404.5:c.*21C>A | ENSP00000477599.2:n.*21C>A | |
| ENST00000649620.1:c.*21C>A | ENSP00000497927.1:n.*21C>A | |
| ENST00000237014.7:c.*21C>A | ENSP00000237014.3:n.*21C>A | |
| ENST00000610404.4:c.*21C>A | ENSP00000477599.1:n.*21C>A | |
| NM_000371.3:c.*21C>A , LRG_416t1:c.*21C>A | NP_000362.1:n.*21C>A | |
| NM_000371.4:c.*21C>A MANE Select | NP_000362.1:n.*21C>A |