Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586412G= , CM000679.2:g.41586412G= | GRCh38 |
| NC_000017.10:g.39742664G= , CM000679.1:g.39742664G= | GRCh37 |
| NC_000017.9:g.36996190G= | NCBI36 |
| NG_008624.1:g.5484C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.423C= MANE Select | ENSP00000167586.6:p.Ala141= | |
| ENST00000167586.6:c.423C= | ENSP00000167586.6:p.Ala141= | |
| NM_000526.4:c.423C= | NP_000517.2:p.Ala141= | |
| NM_000526.5:c.423C= MANE Select | NP_000517.3:p.Ala141= |