Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32056863G>A , CM000668.2:g.32056863G>A | GRCh38 |
| NC_000006.11:g.32024640G>A , CM000668.1:g.32024640G>A | GRCh37 |
| NC_000006.10:g.32132618G>A | NCBI36 |
| NG_008337.2:g.57512C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001365276.2:c.7866C>T MANE Select | NP_001352205.1:p.Thr2622= |
| ENST00000644971.2:c.7866C>T MANE Select | ENSP00000496448.1:p.Thr2622= |
| NM_001365276.1:c.7866C>T | NP_001352205.1:p.Thr2622= |
| NM_019105.6:c.7866C>T | NP_061978.6:p.Thr2622= |
| NM_019105.7:c.7866C>T | NP_061978.6:p.Thr2622= |
| NM_019105.8:c.7866C>T | NP_061978.6:p.Thr2622= |
| ENST00000375244.7:c.7866C>T | ENSP00000364393.3:p.Thr2622= |
| ENST00000611016.2:c.1026C>T | ENSP00000483409.1:p.Thr342= |
| ENST00000647633.1:c.8607C>T | ENSP00000497649.1:p.Thr2869= |