| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127395871C>A , CM000670.2:g.127395871C>A | GRCh38 |
| NC_000008.10:g.128408116C>A , CM000670.1:g.128408116C>A | GRCh37 |
| NC_000008.9:g.128477298C>A | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| NR_117100.1:n.1176+24958G>T (CASC8) | |
| ENST00000645438.1:c.-559-19017C>A (POU5F1B) | ENSP00000495779.1:n.-559-19017C>A |