Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.98723927C>A , CM000675.2:g.98723927C>A | GRCh38 |
| NC_000013.10:g.99376181C>A , CM000675.1:g.99376181C>A | GRCh37 |
| NC_000013.9:g.98174182C>A | NCBI36 |
| NG_017032.1:g.33749G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005073.4:c.350G>T MANE Select | NP_005064.1:p.Ser117Ile |
| ENST00000376503.10:c.350G>T MANE Select | ENSP00000365686.4:p.Ser117Ile |
| NM_005073.3:c.350G>T | NP_005064.1:p.Ser117Ile |
| ENST00000376494.1:n.447G>T | |
| ENST00000376503.9:c.350G>T | ENSP00000365686.4:p.Ser117Ile |
| ENST00000613008.1:c.380G>T | ENSP00000482440.1:p.Ser127Ile |
| ENST00000618992.4:c.350G>T | ENSP00000478051.1:p.Ser117Ile |