Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73367790G= , CM000677.2:g.73367790G= | GRCh38 |
| NC_000015.9:g.73660131G= , CM000677.1:g.73660131G= | GRCh37 |
| NC_000015.8:g.71447184G= | NCBI36 |
| NG_009063.1:g.6475C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.481C= MANE Select | ENSP00000261917.3:p.Pro161= | |
| ENST00000261917.3:c.481C= | ENSP00000261917.3:p.Pro161= | |
| NM_005477.2:c.481C= | NP_005468.1:p.Pro161= | |
| NM_005477.3:c.481C= MANE Select | NP_005468.1:p.Pro161= |