Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586328A= , CM000679.2:g.41586328A= | GRCh38 |
| NC_000017.10:g.39742580A= , CM000679.1:g.39742580A= | GRCh37 |
| NC_000017.9:g.36996106A= | NCBI36 |
| NG_008624.1:g.5568T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.507T= MANE Select | ENSP00000167586.6:p.Ile169= | |
| ENST00000167586.6:c.507T= | ENSP00000167586.6:p.Ile169= | |
| NM_000526.4:c.507T= | NP_000517.2:p.Ile169= | |
| NM_000526.5:c.507T= MANE Select | NP_000517.3:p.Ile169= |