Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075687T= , CM000679.2:g.8075687T= | GRCh38 |
| NC_000017.10:g.7979005T= , CM000679.1:g.7979005T= | GRCh37 |
| NC_000017.9:g.7919730T= | NCBI36 |
| NG_007099.1:g.17017A= | |
| NG_007099.2:g.17030A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001139.3:c.1562A= MANE Select | NP_001130.1:p.Tyr521= |
| ENST00000647874.1:c.1562A= MANE Select | ENSP00000497784.1:p.Tyr521= |
| NM_001139.2:c.1562A= | NP_001130.1:p.Tyr521= |
| ENST00000319144.4:c.1562A= | ENSP00000315167.4:p.Tyr521= |
| ENST00000577351.5:n.479+488A= | |
| ENST00000649809.1:c.626A= | ENSP00000496845.1:p.Tyr209= |