Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124872411C>A , CM000673.2:g.124872411C>A | GRCh38 |
| NC_000011.9:g.124742307C>A , CM000673.1:g.124742307C>A | GRCh37 |
| NC_000011.8:g.124247517C>A | NCBI36 |
| NG_016214.1:g.12003C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397801.6:c.1189C>A MANE Select | ENSP00000380903.1:p.Pro397Thr | |
| ENST00000397801.5:c.1189C>A | ENSP00000380903.1:p.Pro397Thr | |
| ENST00000538940.5:c.1123C>A | ENSP00000441797.1:p.Pro375Thr | |
| NM_022370.3:c.1189C>A | NP_071765.2:p.Pro397Thr | |
| XM_011542953.1:c.2161C>A | XP_011541255.1:p.Pro721Thr | |
| XM_017018122.1:c.1123C>A | XP_016873611.1:p.Pro375Thr | |
| NM_022370.4:c.1189C>A MANE Select | NP_071765.2:p.Pro397Thr |