Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584218T>A , CM000679.2:g.41584218T>A | GRCh38 |
| NC_000017.10:g.39740470T>A , CM000679.1:g.39740470T>A | GRCh37 |
| NC_000017.9:g.36993996T>A | NCBI36 |
| NG_008624.1:g.7678A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.765+39A>T MANE Select | ENSP00000167586.6:n.765+39A>T | |
| ENST00000167586.6:c.765+39A>T | ENSP00000167586.6:n.765+39A>T | |
| ENST00000476662.1:n.215+39A>T | ||
| NM_000526.4:c.765+39A>T | NP_000517.2:n.765+39A>T | |
| NM_000526.5:c.765+39A>T MANE Select | NP_000517.3:n.765+39A>T |