Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52401340C>A , CM000674.2:g.52401340C>A | GRCh38 |
| NC_000012.11:g.52795124C>A , CM000674.1:g.52795124C>A | GRCh37 |
| NC_000012.10:g.51081391C>A | NCBI36 |
| NG_012298.1:g.10053G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_033033.4:c.630G>T MANE Select | NP_149022.3:p.Glu210Asp |
| ENST00000257974.3:c.630G>T MANE Select | ENSP00000257974.3:p.Glu210Asp |
| NM_033033.3:c.630G>T | NP_149022.3:p.Glu210Asp |
| ENST00000257974.2:c.630G>T | ENSP00000257974.2:p.Glu210Asp |