Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12718221A>C , CM000674.2:g.12718221A>C | GRCh38 |
| NC_000012.11:g.12871155A>C , CM000674.1:g.12871155A>C | GRCh37 |
| NC_000012.10:g.12762422A>C | NCBI36 |
| NG_016341.1:g.5854A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000614874.2:c.382A>C | ENSP00000507272.1:p.Thr128Pro | |
| ENST00000682620.1:n.1631-604A>C | ||
| ENST00000684771.1:n.585-604A>C | ||
| ENST00000228872.9:c.382A>C MANE Select | ENSP00000228872.4:p.Thr128Pro | |
| ENST00000228872.8:c.382A>C | ENSP00000228872.4:p.Thr128Pro | |
| ENST00000396340.1:c.382A>C | ENSP00000379629.1:p.Thr128Pro | |
| ENST00000442489.1:c.193+168A>C | ENSP00000407597.1:n.193+168A>C | |
| ENST00000477087.1:n.155-604A>C | ||
| NM_004064.4:c.382A>C | NP_004055.1:p.Thr128Pro | |
| NM_004064.5:c.382A>C MANE Select | NP_004055.1:p.Thr128Pro |