Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586404T= , CM000679.2:g.41586404T= | GRCh38 |
| NC_000017.10:g.39742656T= , CM000679.1:g.39742656T= | GRCh37 |
| NC_000017.9:g.36996182T= | NCBI36 |
| NG_008624.1:g.5492A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000526.5:c.431A= MANE Select | NP_000517.3:p.Glu144= |
| ENST00000167586.7:c.431A= MANE Select | ENSP00000167586.6:p.Glu144= |
| NM_000526.4:c.431A= | NP_000517.2:p.Glu144= |
| ENST00000167586.6:c.431A= | ENSP00000167586.6:p.Glu144= |