| HGVS | Genome Assembly | 
|---|---|
| NC_000024.10:g.19466444C>T , CM000686.2:g.19466444C>T | GRCh38 | 
| NC_000024.9:g.21628330C>T , CM000686.1:g.21628330C>T | GRCh37 | 
| NC_000024.8:g.20087718C>T | NCBI36 | 
| HGVS | Amino-acid Change | 
|---|---|
| NR_002923.2:n.1671+12G>A | |
| NR_033732.1:n.1671+12G>A | |
| ENST00000400605.5:n.1654+12G>A | |
| ENST00000441139.5:n.1671+12G>A | |
| ENST00000513194.1:n.4579G>A | |
| ENST00000650676.1:n.1660+12G>A |