| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.7776629T= , CM000686.2:g.7776629T= | GRCh38 |
| NC_000024.9:g.7644670T= , CM000686.1:g.7644670T= | GRCh37 |
| NC_000024.8:g.7704670T= | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000442584.2:n.492A= | |
| ENST00000455527.5:n.79A= | |
| ENST00000651261.1:n.190A= | |
| ENST00000652723.1:n.1102A= |