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