Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218814652C>T , CM000664.2:g.218814652C>T | GRCh38 |
| NC_000002.11:g.219679375C>T , CM000664.1:g.219679375C>T | GRCh37 |
| NC_000002.10:g.219387619C>T | NCBI36 |
| NG_007959.1:g.37904C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000784.4:c.1371C>T MANE Select | NP_000775.1:p.Thr457= |
| ENST00000258415.9:c.1371C>T MANE Select | ENSP00000258415.4:p.Thr457= |
| NM_000784.3:c.1371C>T | NP_000775.1:p.Thr457= |
| ENST00000258415.8:c.1371C>T | ENSP00000258415.4:p.Thr457= |
| ENST00000494263.5:n.2083C>T | |
| XM_017003488.2:c.951C>T | XP_016858977.1:p.Thr317= |