Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81705535T= , CM000665.2:g.81705535T= | GRCh38 |
| NC_000003.11:g.81754686T= , CM000665.1:g.81754686T= | GRCh37 |
| NC_000003.10:g.81837376T= | NCBI36 |
| NG_011810.1:g.61266A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.222A= MANE Select | ENSP00000410833.2:p.Glu74= | |
| ENST00000429644.6:c.222A= | ENSP00000410833.2:p.Glu74= | |
| ENST00000489715.1:c.99A= | ENSP00000419638.1:p.Glu33= | |
| NM_000158.3:c.222A= | NP_000149.3:p.Glu74= | |
| NM_000158.4:c.222A= MANE Select | NP_000149.4:p.Glu74= |