Linked Data
dbSNP Id:
rs1678046649
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193251743T>G , CM000663.2:g.193251743T>G | GRCh38 |
| NC_000001.10:g.193220873T>G , CM000663.1:g.193220873T>G | GRCh37 |
| NC_000001.9:g.191487496T>G | NCBI36 |
| NG_012691.1:g.134786T>G , LRG_507:g.134786T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367435.5:c.*1031T>G MANE Select | ENSP00000356405.4:n.*1031T>G | |
| ENST00000635846.1:c.*1031T>G | ENSP00000490035.1:n.*1031T>G | |
| ENST00000643006.1:c.*1537T>G | ENSP00000496633.1:n.*1537T>G | |
| ENST00000367435.3:c.*1031T>G | ENSP00000356405.3:n.*1031T>G | |
| NM_024529.4:c.*1031T>G , LRG_507t1:c.*1031T>G | NP_078805.3:n.*1031T>G | |
| NM_024529.5:c.*1031T>G MANE Select | NP_078805.3:n.*1031T>G |