Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173527C>T , CM000678.2:g.173527C>T | GRCh38 |
| NC_000016.9:g.223526C>T , CM000678.1:g.223526C>T | GRCh37 |
| NC_000016.8:g.163526C>T | NCBI36 |
| NG_000006.1:g.34390C>T | |
| NG_059186.1:g.1877C>T | |
| NG_059271.1:g.5681C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.356C>T MANE Select | ENSP00000251595.6:p.Thr119Ile | |
| ENST00000251595.10:c.356C>T | ENSP00000251595.6:p.Thr119Ile | |
| ENST00000397806.1:c.260C>T | ENSP00000380908.1:p.Thr87Ile | |
| ENST00000482565.1:n.492C>T | ||
| NM_000517.4:c.356C>T | NP_000508.1:p.Thr119Ile | |
| NM_000517.6:c.356C>T MANE Select | NP_000508.1:p.Thr119Ile |