Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47332697T= , CM000673.2:g.47332697T= | GRCh38 |
| NC_000011.9:g.47354248T= , CM000673.1:g.47354248T= | GRCh37 |
| NC_000011.8:g.47310824T= | NCBI36 |
| NG_007667.1:g.25006A= , LRG_386:g.25006A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545968.6:c.3496A= MANE Select | ENSP00000442795.1:p.Thr1166= | |
| ENST00000256993.8:c.3496A= | ENSP00000256993.5:p.Thr1166= | |
| ENST00000399249.6:c.3496A= | ENSP00000382193.2:p.Thr1166= | |
| ENST00000545968.5:c.3496A= | ENSP00000442795.1:p.Thr1166= | |
| NM_000256.3:c.3496A= , LRG_386t1:c.3496A= MANE Select | NP_000247.2:p.Thr1166= | |
| XM_011520117.1:c.3478A= | XP_011518419.1:p.Thr1160= | |
| XM_011520118.1:c.3415A= | XP_011518420.1:p.Thr1139= |