Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45097620A>T , CM000677.2:g.45097620A>T | GRCh38 |
| NC_000015.9:g.45389818A>T , CM000677.1:g.45389818A>T | GRCh37 |
| NC_000015.8:g.43177110A>T | NCBI36 |
| NG_009447.1:g.21542T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001363711.2:c.3687T>A MANE Select | NP_001350640.1:p.Tyr1229Ter |
| ENST00000389039.11:c.3687T>A MANE Select | ENSP00000373691.7:p.Tyr1229Ter |
| NM_001363711.1:c.3687T>A | NP_001350640.1:p.Tyr1229Ter |
| NM_014080.4:c.3687T>A | NP_054799.4:p.Tyr1229Ter |
| NM_014080.5:c.3687T>A | NP_054799.4:p.Tyr1229Ter |
| ENST00000389039.10:c.3687T>A | ENSP00000373691.6:p.Tyr1229Ter |
| ENST00000603300.1:c.3687T>A | ENSP00000475084.1:p.Tyr1229Ter |
| XM_005254421.2:c.3687T>A | XP_005254478.1:p.Tyr1229Ter |