Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.98723927C>G , CM000675.2:g.98723927C>G | GRCh38 |
| NC_000013.10:g.99376181C>G , CM000675.1:g.99376181C>G | GRCh37 |
| NC_000013.9:g.98174182C>G | NCBI36 |
| NG_017032.1:g.33749G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005073.4:c.350G>C MANE Select | NP_005064.1:p.Ser117Thr |
| ENST00000376503.10:c.350G>C MANE Select | ENSP00000365686.4:p.Ser117Thr |
| NM_005073.3:c.350G>C | NP_005064.1:p.Ser117Thr |
| ENST00000376494.1:n.447G>C | |
| ENST00000376503.9:c.350G>C | ENSP00000365686.4:p.Ser117Thr |
| ENST00000613008.1:c.380G>C | ENSP00000482440.1:p.Ser127Thr |
| ENST00000618992.4:c.350G>C | ENSP00000478051.1:p.Ser117Thr |