Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.27095651C= , CM000669.2:g.27095651C= | GRCh38 |
| NC_000007.13:g.27135270C= , CM000669.1:g.27135270C= | GRCh37 |
| NC_000007.12:g.27101795C= | NCBI36 |
| NG_011813.1:g.5356G= | |
| NG_033087.1:g.4558C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643460.2:c.262G= MANE Select | ENSP00000494260.2:p.Val88= | |
| ENST00000343060.4:c.262G= | ENSP00000343246.4:p.Val88= | |
| ENST00000355633.5:c.262G= | ENSP00000347851.5:p.Val88= | |
| NM_005522.4:c.262G= | NP_005513.1:p.Val88= | |
| NM_153620.2:c.262G= | NP_705873.2:p.Val88= | |
| NM_005522.5:c.262G= MANE Select | NP_005513.2:p.Val88= | |
| NM_153620.3:c.262G= | NP_705873.3:p.Val88= |