Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31269349A>G , CM000668.2:g.31269349A>G | GRCh38 |
| NC_000006.11:g.31237126A>G , CM000668.1:g.31237126A>G | GRCh37 |
| NC_000006.10:g.31345105A>G | NCBI36 |
| NG_029422.2:g.7783T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.1085T>C MANE Select | ENSP00000365402.5:p.Ile362Thr | |
| ENST00000376228.9:c.1085T>C | ENSP00000365402.5:p.Ile362Thr | |
| ENST00000376237.8:c.*672T>C | ENSP00000365412.4:n.*672T>C | |
| ENST00000383329.7:c.1103T>C | ENSP00000372819.3:p.Ile368Thr | |
| ENST00000466892.5:n.318T>C | ||
| ENST00000470363.5:n.843T>C | ||
| ENST00000487245.5:n.1444T>C | ||
| NM_002117.5:c.1085T>C | NP_002108.4:p.Ile362Thr | |
| NM_002117.6:c.1085T>C MANE Select | NP_002108.4:p.Ile362Thr |