Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270393T>A , CM000668.2:g.31270393T>A | GRCh38 |
| NC_000006.11:g.31238170T>A , CM000668.1:g.31238170T>A | GRCh37 |
| NC_000006.10:g.31346149T>A | NCBI36 |
| NG_029422.2:g.6739A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.712A>T MANE Select | ENSP00000365402.5:p.Thr238Ser | |
| ENST00000376228.9:c.712A>T | ENSP00000365402.5:p.Thr238Ser | |
| ENST00000376237.8:c.*299A>T | ENSP00000365412.4:n.*299A>T | |
| ENST00000383329.7:c.712A>T | ENSP00000372819.3:p.Thr238Ser | |
| ENST00000415537.1:c.664+46A>T | ||
| ENST00000470363.5:n.30A>T | ||
| ENST00000487245.5:n.1071A>T | ||
| ENST00000495835.1:n.901A>T | ||
| NM_002117.5:c.712A>T | NP_002108.4:p.Thr238Ser | |
| NM_002117.6:c.712A>T MANE Select | NP_002108.4:p.Thr238Ser |