Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.176958C>G , CM000678.2:g.176958C>G | GRCh38 |
| NC_000016.9:g.226957C>G , CM000678.1:g.226957C>G | GRCh37 |
| NC_000016.8:g.166957C>G | NCBI36 |
| NG_000006.1:g.37821C>G | |
| NG_059186.1:g.5308C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000558.5:c.125C>G MANE Select | NP_000549.1:p.Thr42Ser |
| ENST00000320868.9:c.125C>G MANE Select | ENSP00000322421.5:p.Thr42Ser |
| NM_000558.4:c.125C>G | NP_000549.1:p.Thr42Ser |
| ENST00000397797.1:c.29C>G | ENSP00000380899.1:p.Thr10Ser |
| ENST00000472694.1:n.261C>G | |
| ENST00000487791.1:n.94C>G |