Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7668315A>T , CM000679.2:g.7668315A>T | GRCh38 |
| NC_000017.10:g.7571633A>T , CM000679.1:g.7571633A>T | GRCh37 |
| NC_000017.9:g.7512358A>T | NCBI36 |
| NG_017013.2:g.24236T>A , LRG_321:g.24236T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000359597.8:c.994-2071T>A | ENSP00000352610.4:n.994-2071T>A |
| ENST00000413465.6:c.782+5866T>A | ENSP00000410739.2:n.782+5866T>A |
| ENST00000635293.1:c.984-890T>A | ENSP00000488924.1:n.984-890T>A |