Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124872919G>T , CM000673.2:g.124872919G>T | GRCh38 |
| NC_000011.9:g.124742815G>T , CM000673.1:g.124742815G>T | GRCh37 |
| NC_000011.8:g.124248025G>T | NCBI36 |
| NG_016214.1:g.12511G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022370.4:c.1366G>T MANE Select | NP_071765.2:p.Gly456Ter |
| ENST00000397801.6:c.1366G>T MANE Select | ENSP00000380903.1:p.Gly456Ter |
| NM_022370.3:c.1366G>T | NP_071765.2:p.Gly456Ter |
| ENST00000397801.5:c.1366G>T | ENSP00000380903.1:p.Gly456Ter |
| ENST00000538940.5:c.1300G>T | ENSP00000441797.1:p.Gly434Ter |
| XM_011542953.1:c.2338G>T | XP_011541255.1:p.Gly780Ter |
| XM_017018122.1:c.1300G>T | XP_016873611.1:p.Gly434Ter |