Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138946165G>A , CM000665.2:g.138946165G>A | GRCh38 |
| NC_000003.11:g.138665007G>A , CM000665.1:g.138665007G>A | GRCh37 |
| NC_000003.10:g.140147697G>A | NCBI36 |
| NG_012454.1:g.5976C>T | |
| NG_029796.1:g.3932G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.558C>T MANE Select | ENSP00000497217.1:p.Tyr186= | |
| ENST00000330315.3:c.558C>T | ENSP00000333188.3:p.Tyr186= | |
| NM_023067.3:c.558C>T | NP_075555.1:p.Tyr186= | |
| NM_023067.4:c.558C>T MANE Select | NP_075555.1:p.Tyr186= |