Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225533T= , CM000668.2:g.3225533T= | GRCh38 |
| NC_000006.11:g.3225767T= , CM000668.1:g.3225767T= | GRCh37 |
| NC_000006.10:g.3170766T= | NCBI36 |
| NG_016715.1:g.7202A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.556A= MANE Select | ENSP00000259818.6:p.Thr186= | |
| ENST00000680070.1:n.1486A= | ||
| ENST00000681707.1:n.1383A= | ||
| ENST00000681757.1:n.861A= | ||
| ENST00000259818.7:c.556A= | ENSP00000259818.6:p.Thr186= | |
| ENST00000473006.1:n.673A= | ||
| NM_178012.4:c.556A= | NP_821080.1:p.Thr186= | |
| XM_011514571.1:c.340A= | XP_011512873.1:p.Thr114= | |
| NM_178012.5:c.556A= MANE Select | NP_821080.1:p.Thr186= |