Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100883185A= , CM000676.2:g.100883185A= | GRCh38 |
| NC_000014.8:g.101349522A= , CM000676.1:g.101349522A= | GRCh37 |
| NC_000014.7:g.100419275A= | NCBI36 |
| NG_045001.1:g.6663T= | |
| NG_045000.5:g.51917A= | |
| NG_045000.6:g.51917A= | |
| NG_045001.2:g.25538T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649591.1:c.1604T= MANE Select | ENSP00000497482.1:p.Phe535= | |
| ENST00000534062.1:c.1604T= | ENSP00000435342.1:p.Phe535= | |
| NM_001134888.2:c.1604T= | NP_001128360.1:p.Phe535= | |
| NM_001134888.3:c.1604T= MANE Select | NP_001128360.1:p.Phe535= |