Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658655C= , CM000682.2:g.10658655C= | GRCh38 |
| NC_000020.10:g.10639303C= , CM000682.1:g.10639303C= | GRCh37 |
| NC_000020.9:g.10587303C= | NCBI36 |
| NG_007496.1:g.20392G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.507G= MANE Select | ENSP00000254958.4:p.Thr169= | |
| ENST00000254958.9:c.507G= | ENSP00000254958.4:p.Thr169= | |
| ENST00000423891.6:n.373G= | ||
| NM_000214.2:c.507G= | NP_000205.1:p.Thr169= | |
| NM_000214.3:c.507G= MANE Select | NP_000205.1:p.Thr169= |