Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40471978C>T , CM000677.2:g.40471978C>T | GRCh38 |
| NC_000015.9:g.40764177C>T , CM000677.1:g.40764177C>T | GRCh37 |
| NC_000015.8:g.38551469C>T | NCBI36 |
| NG_017074.1:g.6018C>T , LRG_600:g.6018C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_130468.4:c.765C>T MANE Select | NP_569735.1:p.Gly255= |
| ENST00000306243.7:c.765C>T MANE Select | ENSP00000307297.6:p.Gly255= |
| NM_130468.3:c.765C>T , LRG_600t1:c.765C>T | NP_569735.1:p.Gly255= |
| ENST00000306243.6:c.765C>T | ENSP00000307297.5:p.Gly255= |
| ENST00000559991.1:c.690C>T | ENSP00000453882.1:p.Gly230= |