Linked Data
dbSNP Id:
rs144391649
gnomAD v2:
4-71896283-A-G
gnomAD v3:
4-71030566-A-G
gnomAD v4:
4-71030566-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.71030566A>G , CM000666.2:g.71030566A>G | GRCh38 |
| NC_000004.11:g.71896283A>G , CM000666.1:g.71896283A>G | GRCh37 |
| NC_000004.10:g.72115147A>G | NCBI36 |
| NG_023303.1:g.42019A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000286648.10:c.*1188A>G MANE Select | ENSP00000286648.5:n.*1188A>G | |
| ENST00000286648.9:c.*1188A>G | ENSP00000286648.5:n.*1188A>G | |
| ENST00000503359.5:c.*1915A>G | ENSP00000426389.1:n.*1915A>G | |
| ENST00000504730.5:c.*1255A>G | ENSP00000425578.1:n.*1255A>G | |
| ENST00000504952.1:c.*1114A>G | ENSP00000421508.1:n.*1114A>G | |
| NM_000788.2:c.*1188A>G | NP_000779.1:n.*1188A>G | |
| NM_000788.3:c.*1188A>G MANE Select | NP_000779.1:n.*1188A>G |