Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.60371336G= , CM000680.2:g.60371336G= | GRCh38 |
| NC_000018.9:g.58038569G= , CM000680.1:g.58038569G= | GRCh37 |
| NC_000018.8:g.56189549G= | NCBI36 |
| NG_016441.1:g.6433C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299766.5:c.*15C= MANE Select | ENSP00000299766.3:n.*15C= | |
| ENST00000299766.4:c.*15C= | ENSP00000299766.3:n.*15C= | |
| NM_005912.2:c.*15C= | NP_005903.2:n.*15C= | |
| NM_005912.3:c.*15C= MANE Select | NP_005903.2:n.*15C= |