Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.97601919C= , CM000672.2:g.97601919C= | GRCh38 |
| NC_000010.10:g.99361676C= , CM000672.1:g.99361676C= | GRCh37 |
| NC_000010.9:g.99351666C= | NCBI36 |
| NG_027922.1:g.22575C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_138413.4:c.763C= MANE Select | NP_612422.2:p.Arg255= |
| ENST00000370646.9:c.763C= MANE Select | ENSP00000359680.4:p.Arg255= |
| NM_001134670.1:c.274C= | NP_001128142.1:p.Arg92= |
| NM_001134670.2:c.274C= | NP_001128142.1:p.Arg92= |
| NM_138413.3:c.763C= | NP_612422.2:p.Arg255= |
| ENST00000370642.4:c.173C= | |
| ENST00000370646.8:c.763C= | ENSP00000359680.4:p.Arg255= |
| ENST00000370647.8:c.274C= | ENSP00000359681.4:p.Arg92= |
| ENST00000370649.3:c.274C= | ENSP00000359683.3:p.Arg92= |