| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.47906043T= , CM000674.2:g.47906043T= | GRCh38 |
| NC_000012.11:g.48299826T= , CM000674.1:g.48299826T= | GRCh37 |
| NC_000012.10:g.46586093T= | NCBI36 |
| NG_008731.1:g.3989A= |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000395324.6:c.-83-23269A= | ENSP00000378734.2:n.-83-23269A= |