Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.99221621C= , CM000671.2:g.99221621C= | GRCh38 |
| NC_000009.11:g.101983903C= , CM000671.1:g.101983903C= | GRCh37 |
| NC_000009.10:g.101023724C= | NCBI36 |
| NG_008928.1:g.5344G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476832.2:c.274G= MANE Select | ENSP00000417764.1:p.Val92= | |
| ENST00000238477.5:c.274G= | ENSP00000432675.2:p.Val92= | |
| ENST00000476832.1:c.274G= | ENSP00000417764.1:p.Val92= | |
| NM_033087.3:c.274G= | NP_149078.1:p.Val92= | |
| NR_024532.1:n.344G= | ||
| NM_033087.4:c.274G= MANE Select | NP_149078.1:p.Val92= | |
| NR_024532.2:n.322G= |