Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4912064T>C , CM000674.2:g.4912064T>C | GRCh38 |
| NC_000012.11:g.5021230T>C , CM000674.1:g.5021230T>C | GRCh37 |
| NC_000012.10:g.4891491T>C | NCBI36 |
| NG_011815.1:g.7158T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382545.5:c.686T>C MANE Select | ENSP00000371985.3:p.Ile229Thr | |
| ENST00000543874.3:n.105+1592T>C | ||
| ENST00000639306.1:c.524T>C | ENSP00000492506.1:p.Ile175Thr | |
| ENST00000382545.3:c.686T>C | ENSP00000371985.3:p.Ile229Thr | |
| ENST00000541095.1:n.105+1592T>C | ||
| ENST00000543874.2:n.96+1592T>C | ||
| NM_000217.2:c.686T>C | NP_000208.2:p.Ile229Thr | |
| NM_000217.3:c.686T>C MANE Select | NP_000208.2:p.Ile229Thr |