Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52519819T>C , CM000674.2:g.52519819T>C | GRCh38 |
| NC_000012.11:g.52913603T>C , CM000674.1:g.52913603T>C | GRCh37 |
| NC_000012.10:g.51199870T>C | NCBI36 |
| NG_008297.1:g.5641A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000252242.9:c.478A>G MANE Select | ENSP00000252242.4:p.Ser160Gly | |
| ENST00000252242.8:c.478A>G | ENSP00000252242.4:p.Ser160Gly | |
| ENST00000549420.1:c.148A>G | ENSP00000447209.1:p.Ser50Gly | |
| ENST00000551275.1:c.373A>G | ENSP00000448041.1:p.Ser125Gly | |
| ENST00000552629.5:n.576A>G | ||
| NM_000424.3:c.478A>G | NP_000415.2:p.Ser160Gly | |
| NM_000424.4:c.478A>G MANE Select | NP_000415.2:p.Ser160Gly |