Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.101753485T= , CM000674.2:g.101753485T= | GRCh38 |
| NC_000012.11:g.102147263T= , CM000674.1:g.102147263T= | GRCh37 |
| NC_000012.10:g.100671394T= | NCBI36 |
| NG_021243.1:g.82383A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299314.12:c.3489A= MANE Select | ENSP00000299314.7:p.Thr1163= | |
| ENST00000299314.11:c.3489A= | ENSP00000299314.7:p.Thr1163= | |
| ENST00000549738.5:c.387A= | ENSP00000450161.1:n.387A= | |
| NM_024312.4:c.3489A= | NP_077288.2:p.Thr1163= | |
| XM_011538731.1:c.3408A= | XP_011537033.1:p.Thr1136= | |
| XM_011538731.2:c.3408A= | XP_011537033.1:p.Thr1136= | |
| XM_017019961.1:c.3273A= | XP_016875450.1:p.Thr1091= | |
| XM_017019962.2:c.2262A= | XP_016875451.1:p.Thr754= | |
| NM_024312.5:c.3489A= MANE Select | NP_077288.2:p.Thr1163= |