Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11965583G>C , CM000663.2:g.11965583G>C | GRCh38 |
| NC_000001.10:g.12025640G>C , CM000663.1:g.12025640G>C | GRCh37 |
| NC_000001.9:g.11948227G>C | NCBI36 |
| NG_008159.1:g.35895G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000196061.5:c.1574G>C MANE Select | ENSP00000196061.4:p.Ser525Thr | |
| ENST00000196061.4:c.1574G>C | ENSP00000196061.4:p.Ser525Thr | |
| ENST00000470133.1:n.188G>C | ||
| ENST00000491536.5:n.202G>C | ||
| NM_000302.3:c.1574G>C | NP_000293.2:p.Ser525Thr | |
| NM_001316320.1:c.1715G>C | NP_001303249.1:p.Ser572Thr | |
| XM_011541594.1:c.1655G>C | XP_011539896.1:p.Ser552Thr | |
| XM_024447707.1:c.908G>C | XP_024303475.1:p.Ser303Thr | |
| NM_000302.4:c.1574G>C MANE Select | NP_000293.2:p.Ser525Thr | |
| NM_001316320.2:c.1715G>C | NP_001303249.1:p.Ser572Thr |