Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122506737C= , CM000672.2:g.122506737C= | GRCh38 |
| NC_000010.10:g.124266253C= , CM000672.1:g.124266253C= | GRCh37 |
| NC_000010.9:g.124256243C= | NCBI36 |
| NG_011554.1:g.50213C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.824C= MANE Select | ENSP00000357980.3:p.Pro275= | |
| ENST00000648167.1:c.506C= | ENSP00000498033.1:p.Pro169= | |
| ENST00000368984.7:c.824C= | ENSP00000357980.3:p.Pro275= | |
| ENST00000420892.1:c.47C= | ENSP00000412676.1:p.Pro16= | |
| NM_002775.4:c.824C= | NP_002766.1:p.Pro275= | |
| NM_002775.5:c.824C= MANE Select | NP_002766.1:p.Pro275= |