Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10127681G= , CM000679.2:g.10127681G= | GRCh38 |
| NC_000017.10:g.10030998G= , CM000679.1:g.10030998G= | GRCh37 |
| NC_000017.9:g.9971723G= | NCBI36 |
| NG_029502.1:g.75871C= | |
| NG_029502.2:g.75871C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432992.7:c.183+70527C= MANE Select | ENSP00000407552.2:n.183+70527C= | |
| ENST00000432992.6:c.183+70527C= | ENSP00000407552.2:n.183+70527C= | |
| NM_201433.1:c.183+70527C= | NP_958839.1:n.183+70527C= | |
| NM_201433.2:c.183+70527C= MANE Select | NP_958839.1:n.183+70527C= |