Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99420702A>G , CM000666.2:g.99420702A>G | GRCh38 |
| NC_000004.11:g.100341859A>G , CM000666.1:g.100341859A>G | GRCh37 |
| NC_000004.10:g.100560882A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437033.7:c.656T>C MANE Select | ENSP00000414254.2:p.Ile219Thr | |
| ENST00000209665.8:c.692T>C | ENSP00000209665.4:p.Ile231Thr | |
| ENST00000437033.6:c.656T>C | ENSP00000414254.2:p.Ile219Thr | |
| ENST00000476959.5:c.716T>C | ENSP00000420269.1:p.Ile239Thr | |
| ENST00000482593.5:c.485T>C | ENSP00000420613.1:p.Ile162Thr | |
| NM_000673.4:c.692T>C | NP_000664.2:p.Ile231Thr | |
| NM_001166504.1:c.716T>C | NP_001159976.1:p.Ile239Thr | |
| NM_000673.7:c.656T>C MANE Select | NP_000664.3:p.Ile219Thr | |
| NM_001166504.2:c.716T>C | NP_001159976.1:p.Ile239Thr |