Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586369G>T , CM000679.2:g.41586369G>T | GRCh38 |
| NC_000017.10:g.39742621G>T , CM000679.1:g.39742621G>T | GRCh37 |
| NC_000017.9:g.36996147G>T | NCBI36 |
| NG_008624.1:g.5527C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000167586.7:c.466C>A MANE Select | ENSP00000167586.6:p.Pro156Thr | |
| ENST00000167586.6:c.466C>A | ENSP00000167586.6:p.Pro156Thr | |
| NM_000526.4:c.466C>A | NP_000517.2:p.Pro156Thr | |
| NM_000526.5:c.466C>A MANE Select | NP_000517.3:p.Pro156Thr |