Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204162046G= , CM000663.2:g.204162046G= | GRCh38 |
| NC_000001.10:g.204131174G= , CM000663.1:g.204131174G= | GRCh37 |
| NC_000001.9:g.202397797G= | NCBI36 |
| NG_012122.1:g.9292C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272190.9:c.216C= MANE Select | ENSP00000272190.8:p.Thr72= | |
| ENST00000638118.1:c.102C= | ENSP00000490307.1:p.Thr34= | |
| ENST00000272190.8:c.216C= | ENSP00000272190.8:p.Thr72= | |
| NM_000537.3:c.216C= | NP_000528.1:p.Thr72= | |
| NM_000537.4:c.216C= MANE Select | NP_000528.1:p.Thr72= |