| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31598649G>T , CM000680.2:g.31598649G>T | GRCh38 |
| NC_000018.9:g.29178612G>T , CM000680.1:g.29178612G>T | GRCh37 |
| NC_000018.8:g.27432610G>T | NCBI36 |
| NG_009490.1:g.11883G>T , LRG_416:g.11883G>T |
| HGVS | Amino-acid Change |
|---|---|
| NM_000371.4:c.418G>T MANE Select | NP_000362.1:p.Ala140Ser |
| ENST00000237014.8:c.418G>T MANE Select | ENSP00000237014.4:p.Ala140Ser |
| NM_000371.3:c.418G>T , LRG_416t1:c.418G>T | NP_000362.1:p.Ala140Ser |
| ENST00000237014.7:c.418G>T | ENSP00000237014.3:p.Ala140Ser |
| ENST00000610404.4:c.532G>T | ENSP00000477599.1:p.Ala178Ser |
| ENST00000610404.5:c.322G>T | ENSP00000477599.2:p.Ala108Ser |
| ENST00000613781.1:c.394G>T | ENSP00000479174.1:p.Ala132Ser |
| ENST00000649620.1:c.418G>T | ENSP00000497927.1:p.Ala140Ser |