Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10647974G>A , CM000682.2:g.10647974G>A | GRCh38 |
| NC_000020.10:g.10628622G>A , CM000682.1:g.10628622G>A | GRCh37 |
| NC_000020.9:g.10576622G>A | NCBI36 |
| NG_007496.1:g.31073C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.1706C>T MANE Select | NP_000205.1:p.Thr569Met |
| ENST00000254958.10:c.1706C>T MANE Select | ENSP00000254958.4:p.Thr569Met |
| NM_000214.2:c.1706C>T | NP_000205.1:p.Thr569Met |
| ENST00000254958.9:c.1706C>T | ENSP00000254958.4:p.Thr569Met |
| ENST00000423891.6:n.1572C>T | |
| ENST00000613518.1:c.55C>T | |
| ENST00000617965.2:n.2295C>T | |
| ENST00000622545.1:c.437C>T |