| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19466453C>T , CM000686.2:g.19466453C>T | GRCh38 |
| NC_000024.9:g.21628339C>T , CM000686.1:g.21628339C>T | GRCh37 |
| NC_000024.8:g.20087727C>T | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| NR_002923.2:n.1671+3G>A | |
| NR_033732.1:n.1671+3G>A | |
| ENST00000400605.5:n.1654+3G>A | |
| ENST00000441139.5:n.1671+3G>A | |
| ENST00000513194.1:n.4570G>A | |
| ENST00000650676.1:n.1660+3G>A |