Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50905475A= , CM000676.2:g.50905475A= | GRCh38 |
| NC_000014.8:g.51372193A= , CM000676.1:g.51372193A= | GRCh37 |
| NC_000014.7:g.50441943A= | NCBI36 |
| NG_012796.1:g.44056T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216392.8:c.2461T= MANE Select | ENSP00000216392.7:p.Tyr821= | |
| ENST00000216392.7:c.2461T= | ENSP00000216392.7:p.Tyr821= | |
| ENST00000532462.5:c.2379+2796T= | ENSP00000431657.1:n.2379+2796T= | |
| ENST00000544180.6:c.2359T= | ENSP00000443787.1:p.Tyr787= | |
| NM_001163940.1:c.2359T= | NP_001157412.1:p.Tyr787= | |
| NM_002863.4:c.2461T= | NP_002854.3:p.Tyr821= | |
| NM_002863.5:c.2461T= MANE Select | NP_002854.3:p.Tyr821= | |
| NM_001163940.2:c.2359T= | NP_001157412.1:p.Tyr787= |