| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.43871283C= , CM000669.2:g.43871283C= | GRCh38 |
| NC_000007.13:g.43910882C= , CM000669.1:g.43910882C= | GRCh37 |
| NC_000007.12:g.43877407C= | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| NM_001204871.1:c.176-1907G= | NP_001191800.1:n.176-1907G= |
| NM_001204871.2:c.176-1907G= | NP_001191800.1:n.176-1907G= |
| ENST00000603700.1:c.176-1907G= | ENSP00000473871.1:n.176-1907G= |