Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65077619G= , CM000677.2:g.65077619G= | GRCh38 |
| NC_000015.9:g.65369957G= , CM000677.1:g.65369957G= | GRCh37 |
| NC_000015.8:g.63157010G= | NCBI36 |
| NG_021411.1:g.5804G= , LRG_682:g.5804G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000432196.5:c.804G= MANE Select | ENSP00000388723.2:p.Gln268= | |
| ENST00000432196.3:c.804G= | ENSP00000388723.2:p.Gln268= | |
| NM_001101362.2:c.804G= , LRG_682t1:c.804G= | NP_001094832.1:p.Gln268= | |
| NM_001101362.3:c.804G= MANE Select | NP_001094832.1:p.Gln268= |