Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17022664G>T , CM000663.2:g.17022664G>T | GRCh38 |
| NC_000001.10:g.17349159G>T , CM000663.1:g.17349159G>T | GRCh37 |
| NC_000001.9:g.17221746G>T | NCBI36 |
| NG_012340.1:g.36507C>A , LRG_316:g.36507C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.538C>A | ENSP00000481376.2:p.Pro180Thr | |
| ENST00000491274.6:c.667C>A | ENSP00000480482.2:p.Pro223Thr | |
| ENST00000375499.8:c.709C>A MANE Select | ENSP00000364649.3:p.Pro237Thr | |
| ENST00000375499.7:c.709C>A | ENSP00000364649.3:p.Pro237Thr | |
| ENST00000475049.5:n.134C>A | ||
| ENST00000485092.5:n.373C>A | ||
| ENST00000485515.5:n.643C>A | ||
| NM_003000.2:c.709C>A , LRG_316t1:c.709C>A | NP_002991.2:p.Pro237Thr | |
| NM_003000.3:c.709C>A MANE Select | NP_002991.2:p.Pro237Thr |