Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6633009C= , CM000673.2:g.6633009C= | GRCh38 |
| NC_000011.9:g.6654240C= , CM000673.1:g.6654240C= | GRCh37 |
| NC_000011.8:g.6610816C= | NCBI36 |
| NG_033858.1:g.27841G= | |
| NG_033858.2:g.27841G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003737.4:c.2503G= MANE Select | NP_003728.1:p.Gly835= |
| ENST00000299441.5:c.2503G= MANE Select | ENSP00000299441.3:p.Gly835= |
| NM_003737.3:c.2503G= | NP_003728.1:p.Gly835= |
| ENST00000299441.4:c.2503G= | ENSP00000299441.3:p.Gly835= |