Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124872544T= , CM000673.2:g.124872544T= | GRCh38 |
| NC_000011.9:g.124742440T= , CM000673.1:g.124742440T= | GRCh37 |
| NC_000011.8:g.124247650T= | NCBI36 |
| NG_016214.1:g.12136T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397801.6:c.1322T= MANE Select | ENSP00000380903.1:p.Ile441= | |
| ENST00000397801.5:c.1322T= | ENSP00000380903.1:p.Ile441= | |
| ENST00000538940.5:c.1256T= | ENSP00000441797.1:p.Ile419= | |
| NM_022370.3:c.1322T= | NP_071765.2:p.Ile441= | |
| XM_011542953.1:c.2294T= | XP_011541255.1:p.Ile765= | |
| XM_017018122.1:c.1256T= | XP_016873611.1:p.Ile419= | |
| NM_022370.4:c.1322T= MANE Select | NP_071765.2:p.Ile441= |