Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65197542T>C , CM000677.2:g.65197542T>C | GRCh38 |
| NC_000015.9:g.65489880T>C , CM000677.1:g.65489880T>C | GRCh37 |
| NC_000015.8:g.63276933T>C | NCBI36 |
| NG_012214.1:g.18961A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003613.4:c.2744A>G MANE Select | NP_003604.4:p.Tyr915Cys |
| ENST00000261883.6:c.2744A>G MANE Select | ENSP00000261883.4:p.Tyr915Cys |
| NM_003613.3:c.2744A>G | NP_003604.3:p.Tyr915Cys |
| ENST00000261883.5:c.2744A>G | ENSP00000261883.4:p.Tyr915Cys |
| XM_017022678.2:c.2825A>G | XP_016878167.1:p.Tyr942Cys |
| XM_017022679.1:c.2672A>G | XP_016878168.1:p.Tyr891Cys |