gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00000365 (SAS)
Exomes Max Group AF
0.00000385 (SAS)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.55191757C>G , CM000669.2:g.55191757C>G | GRCh38 |
| NC_000007.13:g.55259450C>G , CM000669.1:g.55259450C>G | GRCh37 |
| NC_000007.12:g.55226944C>G | NCBI36 |
| NG_007726.3:g.177726C>G , LRG_304:g.177726C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450046.2:c.2349C>G | ENSP00000413354.2:p.Arg783= | |
| ENST00000700145.1:c.857C>G | ||
| ENST00000275493.7:c.2508C>G MANE Select | ENSP00000275493.2:p.Arg836= | |
| ENST00000275493.6:c.2508C>G | ENSP00000275493.2:p.Arg836= | |
| ENST00000442591.5:c.*28+18829C>G | ENSP00000410031.1:n.*28+18829C>G | |
| ENST00000454757.6:c.2373C>G | ENSP00000395243.3:p.Arg791= | |
| ENST00000455089.5:c.2373C>G | ENSP00000415559.1:p.Arg791= | |
| NM_005228.3:c.2508C>G , LRG_304t1:c.2508C>G | NP_005219.2:p.Arg836= | |
| NM_001346897.1:c.2373C>G | NP_001333826.1:p.Arg791= | |
| NM_001346898.1:c.2508C>G | NP_001333827.1:p.Arg836= | |
| NM_001346899.1:c.2373C>G | NP_001333828.1:p.Arg791= | |
| NM_001346900.1:c.2349C>G | NP_001333829.1:p.Arg783= | |
| NM_001346941.1:c.1707C>G | NP_001333870.1:p.Arg569= | |
| NM_005228.4:c.2508C>G | NP_005219.2:p.Arg836= | |
| NM_005228.5:c.2508C>G MANE Select | NP_005219.2:p.Arg836= | |
| NM_001346897.2:c.2373C>G | NP_001333826.1:p.Arg791= | |
| NM_001346898.2:c.2508C>G | NP_001333827.1:p.Arg836= | |
| NM_001346900.2:c.2349C>G | NP_001333829.1:p.Arg783= | |
| NM_001346941.2:c.1707C>G | NP_001333870.1:p.Arg569= | |
| NM_001346899.2:c.2373C>G | NP_001333828.1:p.Arg791= |