Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.24256068C= , CM000676.2:g.24256068C= | GRCh38 |
| NC_000014.8:g.24725274C= , CM000676.1:g.24725274C= | GRCh37 |
| NC_000014.7:g.23795114C= | NCBI36 |
| NG_007150.1:g.12099G= | |
| NG_007150.2:g.12099G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000206765.11:c.1412G= MANE Select | ENSP00000206765.6:p.Cys471= | |
| ENST00000206765.10:c.1412G= | ENSP00000206765.6:p.Cys471= | |
| ENST00000544573.5:c.86G= | ENSP00000439446.1:p.Cys29= | |
| ENST00000559136.1:c.485G= | ENSP00000453337.1:p.Cys162= | |
| NM_000359.2:c.1412G= | NP_000350.1:p.Cys471= | |
| NM_000359.3:c.1412G= MANE Select | NP_000350.1:p.Cys471= |