Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.12695799C= , CM000671.2:g.12695799C= | GRCh38 |
| NC_000009.11:g.12695799C= , CM000671.1:g.12695799C= | GRCh37 |
| NC_000009.10:g.12685799C= | NCBI36 |
| NG_011705.1:g.7414C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000550.3:c.670C= MANE Select | NP_000541.1:p.His224= |
| ENST00000388918.10:c.670C= MANE Select | ENSP00000373570.4:p.His224= |
| NM_000550.2:c.670C= | NP_000541.1:p.His224= |
| ENST00000381136.2:c.5C= | ENSP00000370528.2:p.Ala2= |
| ENST00000388918.9:c.670C= | ENSP00000373570.4:p.His224= |
| XR_001746372.2:n.859C= |