Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154837659A>G , CM000685.2:g.154837659A>G | GRCh38 |
| NC_000023.10:g.154065934A>G , CM000685.1:g.154065934A>G | GRCh37 |
| NC_000023.9:g.153719128A>G | NCBI36 |
| NG_011403.1:g.190065T>C | |
| NG_033065.1:g.2004T>C | |
| NG_011403.2:g.190065T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.6994T>C MANE Select | ENSP00000353393.4:p.Trp2332Arg | |
| ENST00000644698.1:c.727T>C | ENSP00000495706.1:p.Trp243Arg | |
| ENST00000330287.10:c.589T>C | ENSP00000327895.6:p.Trp197Arg | |
| ENST00000360256.8:c.6994T>C | ENSP00000353393.4:p.Trp2332Arg | |
| NM_000132.3:c.6994T>C | NP_000123.1:p.Trp2332Arg | |
| NM_019863.2:c.589T>C | NP_063916.1:p.Trp197Arg | |
| XM_011531126.1:c.6889T>C | XP_011529428.1:p.Trp2297Arg | |
| NM_000132.4:c.6994T>C MANE Select | NP_000123.1:p.Trp2332Arg | |
| NM_019863.3:c.589T>C | NP_063916.1:p.Trp197Arg |