Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.46890026C>T , CM000673.2:g.46890026C>T | GRCh38 |
| NC_000011.9:g.46911577C>T , CM000673.1:g.46911577C>T | GRCh37 |
| NC_000011.8:g.46868153C>T | NCBI36 |
| NG_021394.1:g.33597G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002334.4:c.2010G>A MANE Select | NP_002325.2:p.Thr670= |
| ENST00000378623.6:c.2010G>A MANE Select | ENSP00000367888.1:p.Thr670= |
| NM_002334.3:c.2010G>A | NP_002325.2:p.Thr670= |
| ENST00000378623.5:c.2010G>A | ENSP00000367888.1:p.Thr670= |
| XM_011520102.1:c.2223G>A | XP_011518404.1:p.Thr741= |
| XM_011520103.1:c.1206G>A | XP_011518405.1:p.Thr402= |
| XM_011520103.2:c.1206G>A | XP_011518405.1:p.Thr402= |
| XM_017017734.1:c.2010G>A | XP_016873223.1:p.Thr670= |