Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52519863A>C , CM000674.2:g.52519863A>C | GRCh38 |
| NC_000012.11:g.52913647A>C , CM000674.1:g.52913647A>C | GRCh37 |
| NC_000012.10:g.51199914A>C | NCBI36 |
| NG_008297.1:g.5597T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.434T>G MANE Select | ENSP00000252242.4:p.Val145Gly | |
| ENST00000252242.8:c.434T>G | ENSP00000252242.4:p.Val145Gly | |
| ENST00000549420.1:c.104T>G | ENSP00000447209.1:p.Val35Gly | |
| ENST00000551275.1:c.329T>G | ENSP00000448041.1:p.Val110Gly | |
| ENST00000552629.5:n.532T>G | ||
| NM_000424.3:c.434T>G | NP_000415.2:p.Val145Gly | |
| NM_000424.4:c.434T>G MANE Select | NP_000415.2:p.Val145Gly |