Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124872539G= , CM000673.2:g.124872539G= | GRCh38 |
| NC_000011.9:g.124742435G= , CM000673.1:g.124742435G= | GRCh37 |
| NC_000011.8:g.124247645G= | NCBI36 |
| NG_016214.1:g.12131G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397801.6:c.1317G= MANE Select | ENSP00000380903.1:p.Leu439= | |
| ENST00000397801.5:c.1317G= | ENSP00000380903.1:p.Leu439= | |
| ENST00000538940.5:c.1251G= | ENSP00000441797.1:p.Leu417= | |
| NM_022370.3:c.1317G= | NP_071765.2:p.Leu439= | |
| XM_011542953.1:c.2289G= | XP_011541255.1:p.Leu763= | |
| XM_017018122.1:c.1251G= | XP_016873611.1:p.Leu417= | |
| NM_022370.4:c.1317G= MANE Select | NP_071765.2:p.Leu439= |