| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31598638A>C , CM000680.2:g.31598638A>C | GRCh38 |
| NC_000018.9:g.29178601A>C , CM000680.1:g.29178601A>C | GRCh37 |
| NC_000018.8:g.27432599A>C | NCBI36 |
| NG_009490.1:g.11872A>C , LRG_416:g.11872A>C |
| HGVS | Amino-acid Change |
|---|---|
| NM_000371.4:c.407A>C MANE Select | NP_000362.1:p.Tyr136Ser |
| ENST00000237014.8:c.407A>C MANE Select | ENSP00000237014.4:p.Tyr136Ser |
| NM_000371.3:c.407A>C , LRG_416t1:c.407A>C | NP_000362.1:p.Tyr136Ser |
| ENST00000237014.7:c.407A>C | ENSP00000237014.3:p.Tyr136Ser |
| ENST00000610404.4:c.521A>C | ENSP00000477599.1:p.Tyr174Ser |
| ENST00000610404.5:c.311A>C | ENSP00000477599.2:p.Tyr104Ser |
| ENST00000613781.1:c.383A>C | ENSP00000479174.1:p.Tyr128Ser |
| ENST00000649620.1:c.407A>C | ENSP00000497927.1:p.Tyr136Ser |