Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41583649T>G , CM000679.2:g.41583649T>G | GRCh38 |
| NC_000017.10:g.39739901T>G , CM000679.1:g.39739901T>G | GRCh37 |
| NC_000017.9:g.36993427T>G | NCBI36 |
| NG_008624.1:g.8247A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.955A>C MANE Select | ENSP00000167586.6:p.Thr319Pro | |
| ENST00000167586.6:c.955A>C | ENSP00000167586.6:p.Thr319Pro | |
| ENST00000476662.1:n.405A>C | ||
| NM_000526.4:c.955A>C | NP_000517.2:p.Thr319Pro | |
| NM_000526.5:c.955A>C MANE Select | NP_000517.3:p.Thr319Pro |