Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12718222C>G , CM000674.2:g.12718222C>G | GRCh38 |
| NC_000012.11:g.12871156C>G , CM000674.1:g.12871156C>G | GRCh37 |
| NC_000012.10:g.12762423C>G | NCBI36 |
| NG_016341.1:g.5855C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000614874.2:c.383C>G | ENSP00000507272.1:p.Thr128Arg | |
| ENST00000682620.1:n.1631-603C>G | ||
| ENST00000684771.1:n.585-603C>G | ||
| ENST00000228872.9:c.383C>G MANE Select | ENSP00000228872.4:p.Thr128Arg | |
| ENST00000228872.8:c.383C>G | ENSP00000228872.4:p.Thr128Arg | |
| ENST00000396340.1:c.383C>G | ENSP00000379629.1:p.Thr128Arg | |
| ENST00000442489.1:c.193+169C>G | ENSP00000407597.1:n.193+169C>G | |
| ENST00000477087.1:n.155-603C>G | ||
| NM_004064.4:c.383C>G | NP_004055.1:p.Thr128Arg | |
| NM_004064.5:c.383C>G MANE Select | NP_004055.1:p.Thr128Arg |