Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48981515T= , CM000674.2:g.48981515T= | GRCh38 |
| NC_000012.11:g.49375298T= , CM000674.1:g.49375298T= | GRCh37 |
| NC_000012.10:g.47661565T= | NCBI36 |
| NG_033141.1:g.8063T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293549.4:c.988T= MANE Select | ENSP00000293549.3:p.Cys330= | |
| ENST00000293549.3:c.988T= | ENSP00000293549.3:p.Cys330= | |
| ENST00000613114.4:c.955T= | ENSP00000481240.1:p.Cys319= | |
| NM_005430.3:c.988T= | NP_005421.1:p.Cys330= | |
| NM_005430.4:c.988T= MANE Select | NP_005421.1:p.Cys330= |