Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204162058T>G , CM000663.2:g.204162058T>G | GRCh38 |
| NC_000001.10:g.204131186T>G , CM000663.1:g.204131186T>G | GRCh37 |
| NC_000001.9:g.202397809T>G | NCBI36 |
| NG_012122.1:g.9280A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000537.4:c.204A>C MANE Select | NP_000528.1:p.Thr68= |
| ENST00000272190.9:c.204A>C MANE Select | ENSP00000272190.8:p.Thr68= |
| NM_000537.3:c.204A>C | NP_000528.1:p.Thr68= |
| ENST00000272190.8:c.204A>C | ENSP00000272190.8:p.Thr68= |
| ENST00000638118.1:c.90A>C | ENSP00000490307.1:p.Thr30= |