Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47284514G>T , CM000679.2:g.47284514G>T | GRCh38 |
| NC_000017.10:g.45361880G>T , CM000679.1:g.45361880G>T | GRCh37 |
| NC_000017.9:g.42716879G>T | NCBI36 |
| NG_008332.2:g.35673G>T , LRG_481:g.35673G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.433G>T | ENSP00000513002.1:p.Asp145Tyr | |
| ENST00000559488.7:c.433G>T MANE Select | ENSP00000452786.2:p.Asp145Tyr | |
| ENST00000559488.5:c.433G>T | ENSP00000452786.1:p.Asp145Tyr | |
| ENST00000560629.1:c.398G>T | ||
| ENST00000571680.1:c.433G>T | ENSP00000461626.1:p.Asp145Tyr | |
| NM_000212.2:c.433G>T , LRG_481t1:c.433G>T | NP_000203.2:p.Asp145Tyr | |
| NM_000212.3:c.433G>T MANE Select | NP_000203.2:p.Asp145Tyr |