Linked Data
dbSNP Id:
rs369968241
ExAC:
20:43248893 T / G
gnomAD v2:
20-43248893-T-G
gnomAD v3:
20-44620252-T-G
gnomAD v4:
20-44620252-T-G
MyVariant Identifiers:
chr20:g.43248893T>G (hg19)
chr20:g.43248893_43248894delinsGG (hg19)
chr20:g.44620252T>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44620252T>G , CM000682.2:g.44620252T>G | GRCh38 |
| NC_000020.10:g.43248893T>G , CM000682.1:g.43248893T>G | GRCh37 |
| NC_000020.9:g.42682307T>G | NCBI36 |
| NG_007385.1:g.36484A>C , LRG_16:g.36484A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000492931.6:n.1245+47A>C (ADA) | ||
| ENST00000536076.2:c.925+47A>C (ADA) | ENSP00000512234.1:n.925+47A>C | |
| ENST00000536532.6:c.*221+47A>C (ADA) | ENSP00000440946.1:n.*221+47A>C | |
| ENST00000537820.2:c.1006+47A>C (ADA) | ENSP00000441818.1:n.1006+47A>C | |
| ENST00000539235.6:c.*462+47A>C (ADA) | ENSP00000446464.1:n.*462+47A>C | |
| ENST00000695889.1:c.553+47A>C (ADA) | ENSP00000512240.1:n.553+47A>C | |
| ENST00000695890.1:n.5236A>C (ADA) | ||
| ENST00000695891.1:c.618+47A>C (ADA) | ENSP00000512241.1:n.618+47A>C | |
| ENST00000695927.1:c.1156+47A>C (ADA) | ENSP00000512270.1:n.1156+47A>C | |
| ENST00000695949.1:c.1003+47A>C (ADA) | ENSP00000512281.1:n.1003+47A>C | |
| ENST00000695956.1:c.233+47A>C (ADA) | ||
| ENST00000695957.1:c.*569+47A>C (ADA) | ENSP00000512286.1:n.*569+47A>C | |
| ENST00000695991.1:c.616+47A>C (ADA) | ENSP00000512314.1:n.616+47A>C | |
| ENST00000695992.1:c.*268A>C (ADA) | ENSP00000512315.1:n.*268A>C | |
| ENST00000695993.1:c.1078+47A>C (ADA) | ENSP00000512316.1:n.1078+47A>C | |
| ENST00000695994.1:c.*221+47A>C (ADA) | ENSP00000512317.1:n.*221+47A>C | |
| ENST00000695995.1:c.688+47A>C (ADA) | ENSP00000512318.1:n.688+47A>C | |
| ENST00000695996.1:n.1160+47A>C (ADA) | ||
| ENST00000696003.1:n.2862+47A>C (ADA) | ||
| ENST00000696004.1:n.1909A>C (ADA) | ||
| ENST00000696005.1:c.575A>C (ADA) | ||
| ENST00000696006.1:c.*221+47A>C (ADA) | ENSP00000512325.1:n.*221+47A>C | |
| ENST00000696007.1:c.1005+47A>C (ADA) | ENSP00000512326.1:n.1005+47A>C | |
| ENST00000696008.1:n.3479A>C (ADA) | ||
| ENST00000696017.1:c.1122A>C (ADA) | ENSP00000512333.1:p.Pro374= | |
| ENST00000696034.1:c.*221+47A>C (ADA) | ENSP00000512343.1:n.*221+47A>C | |
| ENST00000696035.1:n.1311A>C (ADA) | ||
| ENST00000696036.1:n.1826A>C (ADA) | ||
| ENST00000696037.1:n.2755+47A>C (ADA) | ||
| ENST00000696038.1:c.*882A>C (ADA) | ENSP00000512344.1:n.*882A>C | |
| ENST00000696039.1:n.1442+47A>C (ADA) | ||
| ENST00000696058.1:c.1075+47A>C (ADA) | ENSP00000512361.1:n.1075+47A>C | |
| ENST00000696059.1:c.*1023+47A>C (ADA) | ENSP00000512362.1:n.*1023+47A>C | |
| ENST00000696060.1:c.1147+47A>C (ADA) | ENSP00000512363.1:n.1147+47A>C | |
| ENST00000696061.1:c.1075+47A>C (ADA) | ENSP00000512364.1:n.1075+47A>C | |
| ENST00000696062.1:c.1141+47A>C (ADA) | ENSP00000512365.1:n.1141+47A>C | |
| ENST00000696063.1:c.1153+47A>C (ADA) | ENSP00000512366.1:n.1153+47A>C | |
| ENST00000696064.1:c.925+47A>C (ADA) | ENSP00000512367.1:n.925+47A>C | |
| ENST00000696065.1:c.400+47A>C (ADA) | ENSP00000512368.1:n.400+47A>C | |
| ENST00000696072.1:n.480A>C (ADA) | ||
| ENST00000696073.1:n.1389+47A>C (ADA) | ||
| ENST00000696074.1:n.629+47A>C (ADA) | ||
| ENST00000696075.1:c.*1048+47A>C (ADA) | ENSP00000512374.1:n.*1048+47A>C | |
| ENST00000696076.1:c.1194A>C (ADA) | ENSP00000512375.1:p.Pro398= | |
| ENST00000696077.1:c.1072+47A>C (ADA) | ENSP00000512376.1:n.1072+47A>C | |
| ENST00000696078.1:c.1075+47A>C (ADA) | ENSP00000512377.1:n.1075+47A>C | |
| ENST00000696079.1:c.1075+47A>C (ADA) | ENSP00000512378.1:n.1075+47A>C | |
| ENST00000696080.1:c.1078+47A>C (ADA) | ENSP00000512379.1:n.1078+47A>C | |
| ENST00000696081.1:n.1244A>C (ADA) | ||
| ENST00000696082.1:c.1153+47A>C (ADA) | ENSP00000512380.1:n.1153+47A>C | |
| ENST00000696083.1:n.2035+47A>C (ADA) | ||
| ENST00000696084.1:n.1302A>C (ADA) | ||
| ENST00000696104.1:c.*147+47A>C (ADA) | ENSP00000512399.1:n.*147+47A>C | |
| ENST00000372874.9:c.1078+47A>C (ADA) MANE Select | ENSP00000361965.4:n.1078+47A>C | |
| ENST00000372874.8:c.1078+47A>C (ADA) | ENSP00000361965.4:n.1078+47A>C | |
| ENST00000372887.5:c.152-3681T>G (PKIG) | ENSP00000361978.1:n.152-3681T>G | |
| ENST00000464097.5:n.1444+47A>C (ADA) | ||
| ENST00000492931.5:n.1238+47A>C (ADA) | ||
| ENST00000536532.5:c.*221+47A>C (ADA) | ENSP00000440946.1:n.*221+47A>C | |
| ENST00000537820.1:c.1006+47A>C (ADA) | ENSP00000441818.1:n.1006+47A>C | |
| ENST00000539235.5:c.*462+47A>C (ADA) | ENSP00000446464.1:n.*462+47A>C | |
| NM_000022.2:c.1078+47A>C , LRG_16t1:c.1078+47A>C (ADA) | NP_000013.2:n.1078+47A>C | |
| XM_005260236.2:c.1006+47A>C (ADA) | XP_005260293.1:n.1006+47A>C | |
| XM_011528478.1:c.673+47A>C (ADA) | XP_011526780.1:n.673+47A>C | |
| XM_011528479.1:c.673+47A>C (ADA) | XP_011526781.1:n.673+47A>C | |
| XR_244129.1:n.1067+47A>C (ADA) | ||
| NM_000022.3:c.1078+47A>C (ADA) | NP_000013.2:n.1078+47A>C | |
| NM_001322050.1:c.673+47A>C (ADA) | NP_001308979.1:n.673+47A>C | |
| NM_001322051.1:c.1006+47A>C (ADA) | NP_001308980.1:n.1006+47A>C | |
| NR_136160.1:n.1164+47A>C (ADA) | ||
| NM_000022.4:c.1078+47A>C (ADA) MANE Select | NP_000013.2:n.1078+47A>C | |
| NM_001322050.2:c.673+47A>C (ADA) | NP_001308979.1:n.673+47A>C | |
| NM_001322051.2:c.1006+47A>C (ADA) | NP_001308980.1:n.1006+47A>C | |
| NR_136160.2:n.1105+47A>C (ADA) |