Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102835297G>A , CM000672.2:g.102835297G>A | GRCh38 |
| NC_000010.10:g.104595054G>A , CM000672.1:g.104595054G>A | GRCh37 |
| NC_000010.9:g.104585044G>A | NCBI36 |
| NG_007955.1:g.7237C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369887.4:c.393C>T MANE Select | ENSP00000358903.3:p.Thr131= | |
| ENST00000638190.1:c.393C>T | ENSP00000492539.1:p.Thr131= | |
| ENST00000638272.1:c.297+1768C>T | ENSP00000491508.1:n.297+1768C>T | |
| ENST00000638971.1:c.393C>T | ENSP00000492313.1:p.Thr131= | |
| ENST00000639393.1:c.393C>T | ENSP00000492651.1:p.Thr131= | |
| ENST00000640633.1:n.155C>T | ||
| ENST00000369887.3:c.393C>T | ENSP00000358903.3:p.Thr131= | |
| ENST00000489268.1:n.647C>T | ||
| NM_000102.3:c.393C>T | NP_000093.1:p.Thr131= | |
| NM_000102.4:c.393C>T MANE Select | NP_000093.1:p.Thr131= |