Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225555C= , CM000668.2:g.3225555C= | GRCh38 |
| NC_000006.11:g.3225789C= , CM000668.1:g.3225789C= | GRCh37 |
| NC_000006.10:g.3170788C= | NCBI36 |
| NG_016715.1:g.7180G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.534G= MANE Select | ENSP00000259818.6:p.Thr178= | |
| ENST00000680070.1:n.1464G= | ||
| ENST00000681707.1:n.1361G= | ||
| ENST00000681757.1:n.839G= | ||
| ENST00000259818.7:c.534G= | ENSP00000259818.6:p.Thr178= | |
| ENST00000473006.1:n.651G= | ||
| NM_178012.4:c.534G= | NP_821080.1:p.Thr178= | |
| XM_011514571.1:c.318G= | XP_011512873.1:p.Thr106= | |
| NM_178012.5:c.534G= MANE Select | NP_821080.1:p.Thr178= |