Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189062866G>C , CM000664.2:g.189062866G>C | GRCh38 |
| NC_000002.11:g.189927592G>C , CM000664.1:g.189927592G>C | GRCh37 |
| NC_000002.10:g.189635837G>C | NCBI36 |
| NG_011799.1:g.122014C>G | |
| NG_011799.2:g.122014C>G | |
| NG_011799.3:g.167436C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.1976C>G MANE Select | ENSP00000364000.3:p.Pro659Arg | |
| ENST00000374866.7:c.1976C>G | ENSP00000364000.3:p.Pro659Arg | |
| ENST00000470524.2:n.82C>G | ||
| ENST00000618828.1:c.815C>G | ENSP00000482184.1:p.Pro272Arg | |
| NM_000393.3:c.1976C>G | NP_000384.2:p.Pro659Arg | |
| XM_011510573.1:c.1838C>G | XP_011508875.1:p.Pro613Arg | |
| NM_000393.4:c.1976C>G | NP_000384.2:p.Pro659Arg | |
| XM_011510573.3:c.1838C>G | XP_011508875.1:p.Pro613Arg | |
| NM_000393.5:c.1976C>G MANE Select | NP_000384.2:p.Pro659Arg |