Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10646959G>A , CM000682.2:g.10646959G>A | GRCh38 |
| NC_000020.10:g.10627607G>A , CM000682.1:g.10627607G>A | GRCh37 |
| NC_000020.9:g.10575607G>A | NCBI36 |
| NG_007496.1:g.32088C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.1865C>T MANE Select | NP_000205.1:p.Thr622Met |
| ENST00000254958.10:c.1865C>T MANE Select | ENSP00000254958.4:p.Thr622Met |
| NM_000214.2:c.1865C>T | NP_000205.1:p.Thr622Met |
| ENST00000254958.9:c.1865C>T | ENSP00000254958.4:p.Thr622Met |
| ENST00000423891.6:n.1731C>T | |
| ENST00000612857.1:n.354C>T | |
| ENST00000613518.1:c.214C>T | |
| ENST00000617965.2:n.2454C>T |