Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.60372111T= , CM000680.2:g.60372111T= | GRCh38 |
| NC_000018.9:g.58039344T= , CM000680.1:g.58039344T= | GRCh37 |
| NC_000018.8:g.56190324T= | NCBI36 |
| NG_016441.1:g.5658A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299766.5:c.239A= MANE Select | ENSP00000299766.3:p.Tyr80= | |
| ENST00000299766.4:c.239A= | ENSP00000299766.3:p.Tyr80= | |
| NM_005912.2:c.239A= | NP_005903.2:p.Tyr80= | |
| NM_005912.3:c.239A= MANE Select | NP_005903.2:p.Tyr80= |