Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119414294A= , CM000665.2:g.119414294A= | GRCh38 |
| NC_000003.11:g.119133141A= , CM000665.1:g.119133141A= | GRCh37 |
| NC_000003.10:g.120615831A= | NCBI36 |
| NG_007665.2:g.124922A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.2365A= MANE Select | ENSP00000264245.4:p.Thr789= | |
| ENST00000264245.8:c.2365A= | ENSP00000264245.4:p.Thr789= | |
| NM_020754.3:c.2365A= | NP_065805.2:p.Thr789= | |
| XM_005247671.3:c.2272A= | XP_005247728.1:p.Thr758= | |
| XM_006713714.2:c.2305A= | XP_006713777.1:p.Thr769= | |
| XM_006713714.3:c.2305A= | XP_006713777.1:p.Thr769= | |
| XM_017006955.1:c.1873A= | XP_016862444.1:p.Thr625= | |
| NM_020754.4:c.2365A= MANE Select | NP_065805.2:p.Thr789= |