Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270261T>C , CM000668.2:g.31270261T>C | GRCh38 |
| NC_000006.11:g.31238038T>C , CM000668.1:g.31238038T>C | GRCh37 |
| NC_000006.10:g.31346017T>C | NCBI36 |
| NG_029422.2:g.6871A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.844A>G MANE Select | ENSP00000365402.5:p.Thr282Ala | |
| ENST00000376228.9:c.844A>G | ENSP00000365402.5:p.Thr282Ala | |
| ENST00000376237.8:c.*431A>G | ENSP00000365412.4:n.*431A>G | |
| ENST00000383329.7:c.844A>G | ENSP00000372819.3:p.Thr282Ala | |
| ENST00000415537.1:c.735A>G | ||
| ENST00000470363.5:n.162A>G | ||
| ENST00000487245.5:n.1203A>G | ||
| ENST00000495835.1:n.1033A>G | ||
| NM_002117.5:c.844A>G | NP_002108.4:p.Thr282Ala | |
| NM_002117.6:c.844A>G MANE Select | NP_002108.4:p.Thr282Ala |