| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.28621375A>T , CM000670.2:g.28621375A>T | GRCh38 |
| NC_000008.10:g.28478892A>T , CM000670.1:g.28478892A>T | GRCh37 |
| NC_000008.9:g.28534811A>T | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000522725.5:n.314+13617A>T | |
| XM_024447096.1:c.-570+13617A>T | XP_024302864.1:n.-570+13617A>T |
| XR_949615.1:n.364A>T |