Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.24256068C>T , CM000676.2:g.24256068C>T | GRCh38 |
| NC_000014.8:g.24725274C>T , CM000676.1:g.24725274C>T | GRCh37 |
| NC_000014.7:g.23795114C>T | NCBI36 |
| NG_007150.1:g.12099G>A | |
| NG_007150.2:g.12099G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000206765.11:c.1412G>A MANE Select | ENSP00000206765.6:p.Cys471Tyr | |
| ENST00000206765.10:c.1412G>A | ENSP00000206765.6:p.Cys471Tyr | |
| ENST00000544573.5:c.86G>A | ENSP00000439446.1:p.Cys29Tyr | |
| ENST00000559136.1:c.485G>A | ENSP00000453337.1:p.Cys162Tyr | |
| NM_000359.2:c.1412G>A | NP_000350.1:p.Cys471Tyr | |
| NM_000359.3:c.1412G>A MANE Select | NP_000350.1:p.Cys471Tyr |