Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39954436T>A , CM000679.2:g.39954436T>A | GRCh38 |
| NC_000017.10:g.38110689T>A , CM000679.1:g.38110689T>A | GRCh37 |
| NC_000017.9:g.35364215T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000635792.1:c.-6+1131T>A | ENSP00000490739.1:n.-6+1131T>A |