| HGVS | Genome Assembly | 
|---|---|
| NC_000008.11:g.127397266G>C , CM000670.2:g.127397266G>C | GRCh38 | 
| NC_000008.10:g.128409511G>C , CM000670.1:g.128409511G>C | GRCh37 | 
| NC_000008.9:g.128478693G>C | NCBI36 | 
| HGVS | Amino-acid Change | 
|---|---|
| NR_117100.1:n.1176+23563C>G (CASC8) | |
| ENST00000645438.1:c.-559-17622G>C (POU5F1B) | ENSP00000495779.1:n.-559-17622G>C |