| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.32337136C>T , CM000669.2:g.32337136C>T | GRCh38 |
| NC_000007.13:g.32376748C>T , CM000669.1:g.32376748C>T | GRCh37 |
| NC_000007.12:g.32343273C>T | NCBI36 |
| NG_051183.1:g.96089G>A |
| HGVS | Amino-acid Change |
|---|---|
| NM_001322059.1:c.310+90686G>A | NP_001308988.1:n.310+90686G>A |
| NM_001322059.2:c.310+90686G>A | NP_001308988.1:n.310+90686G>A |
| ENST00000672256.1:c.310+90686G>A | ENSP00000499831.1:n.310+90686G>A |