Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118168739C= , CM000673.2:g.118168739C= | GRCh38 |
| NC_000011.9:g.118039454C= , CM000673.1:g.118039454C= | GRCh37 |
| NC_000011.8:g.117544664C= | NCBI36 |
| NG_042217.1:g.12884G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004588.5:c.83G= MANE Select | NP_004579.1:p.Arg28= |
| ENST00000278947.6:c.83G= MANE Select | ENSP00000278947.5:p.Arg28= |
| NM_004588.4:c.83G= | NP_004579.1:p.Arg28= |
| ENST00000278947.5:c.83G= | ENSP00000278947.5:p.Arg28= |
| ENST00000658882.1:c.187G= | ENSP00000499572.1:p.Gly63= |
| ENST00000665446.1:n.319G= | |
| ENST00000669850.1:n.325G= |