Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.119320785G>C , CM000666.2:g.119320785G>C | GRCh38 |
| NC_000004.11:g.120241940G>C , CM000666.1:g.120241940G>C | GRCh37 |
| NC_000004.10:g.120461388G>C | NCBI36 |
| NG_011444.1:g.6377C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274024.4:c.125C>G MANE Select | ENSP00000274024.3:p.Thr42Arg | |
| ENST00000274024.3:c.125C>G | ENSP00000274024.3:p.Thr42Arg | |
| NM_000134.3:c.125C>G | NP_000125.2:p.Thr42Arg | |
| NM_000134.4:c.125C>G MANE Select | NP_000125.2:p.Thr42Arg |