Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.93997881T= , CM000663.2:g.93997881T= | GRCh38 |
| NC_000001.10:g.94463437T= , CM000663.1:g.94463437T= | GRCh37 |
| NC_000001.9:g.94236025T= | NCBI36 |
| NG_009073.1:g.128269A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6709A= MANE Select | ENSP00000359245.3:p.Thr2237= | |
| ENST00000370225.3:c.6709A= | ENSP00000359245.3:p.Thr2237= | |
| ENST00000536513.5:c.3085A= | ENSP00000439707.2:p.Thr1029= | |
| NM_000350.2:c.6709A= | NP_000341.2:p.Thr2237= | |
| NM_000350.3:c.6709A= MANE Select | NP_000341.2:p.Thr2237= |