Linked Data
dbSNP Id:
rs1740666649
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.71030549C>G , CM000666.2:g.71030549C>G | GRCh38 |
| NC_000004.11:g.71896266C>G , CM000666.1:g.71896266C>G | GRCh37 |
| NC_000004.10:g.72115130C>G | NCBI36 |
| NG_023303.1:g.42002C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000286648.10:c.*1171C>G MANE Select | ENSP00000286648.5:n.*1171C>G | |
| ENST00000286648.9:c.*1171C>G | ENSP00000286648.5:n.*1171C>G | |
| ENST00000503359.5:c.*1898C>G | ENSP00000426389.1:n.*1898C>G | |
| ENST00000504730.5:c.*1238C>G | ENSP00000425578.1:n.*1238C>G | |
| ENST00000504952.1:c.*1097C>G | ENSP00000421508.1:n.*1097C>G | |
| NM_000788.2:c.*1171C>G | NP_000779.1:n.*1171C>G | |
| NM_000788.3:c.*1171C>G MANE Select | NP_000779.1:n.*1171C>G |