Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122462001C>T , CM000672.2:g.122462001C>T | GRCh38 |
| NC_000010.10:g.124221517C>T , CM000672.1:g.124221517C>T | GRCh37 |
| NC_000010.9:g.124211507C>T | NCBI36 |
| NG_011554.1:g.5477C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.349C>T MANE Select | ENSP00000357980.3:p.Pro117Ser | |
| ENST00000648167.1:c.154+3292C>T | ENSP00000498033.1:n.154+3292C>T | |
| ENST00000368984.7:c.349C>T | ENSP00000357980.3:p.Pro117Ser | |
| NM_002775.4:c.349C>T | NP_002766.1:p.Pro117Ser | |
| NM_002775.5:c.349C>T MANE Select | NP_002766.1:p.Pro117Ser |