| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.142670446G>A , CM000670.2:g.142670446G>A | GRCh38 |
| NC_000008.10:g.143751864G>A , CM000670.1:g.143751864G>A | GRCh37 |
| NC_000008.9:g.143748866G>A | NCBI36 |
| NG_012215.2:g.4538C>T | |
| NG_011722.3:g.5139G>A |
| HGVS | Amino-acid Change |
|---|---|
| NR_033343.1:n.139G>A (PSCA) | |
| NR_033343.2:n.150G>A (PSCA) | |
| ENST00000505305.1:n.139G>A (PSCA) | |
| ENST00000510969.1:n.126G>A (PSCA) | |
| ENST00000591357.5:n.265-314C>T (JRK) |