Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119414067C= , CM000665.2:g.119414067C= | GRCh38 |
| NC_000003.11:g.119132914C= , CM000665.1:g.119132914C= | GRCh37 |
| NC_000003.10:g.120615604C= | NCBI36 |
| NG_007665.2:g.124695C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.2138C= MANE Select | ENSP00000264245.4:p.Thr713= | |
| ENST00000264245.8:c.2138C= | ENSP00000264245.4:p.Thr713= | |
| NM_020754.3:c.2138C= | NP_065805.2:p.Thr713= | |
| XM_005247671.3:c.2045C= | XP_005247728.1:p.Thr682= | |
| XM_006713714.2:c.2078C= | XP_006713777.1:p.Thr693= | |
| XM_006713714.3:c.2078C= | XP_006713777.1:p.Thr693= | |
| XM_017006955.1:c.1646C= | XP_016862444.1:p.Thr549= | |
| NM_020754.4:c.2138C= MANE Select | NP_065805.2:p.Thr713= |