Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.66228126T= , CM000679.2:g.66228126T= | GRCh38 |
| NC_000017.10:g.64224244T= , CM000679.1:g.64224244T= | GRCh37 |
| NC_000017.9:g.61654706T= | NCBI36 |
| NG_012045.1:g.6313A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000205948.11:c.135A= MANE Select | ENSP00000205948.6:p.Glu45= | |
| ENST00000205948.10:c.135A= | ENSP00000205948.6:p.Glu45= | |
| ENST00000577982.1:c.135A= | ENSP00000464301.1:p.Glu45= | |
| ENST00000581797.5:c.-46A= | ENSP00000463553.1:n.-46A= | |
| NM_000042.2:c.135A= | NP_000033.2:p.Glu45= | |
| NM_000042.3:c.135A= MANE Select | NP_000033.2:p.Glu45= |