Linked Data
ClinVar Variation Id:
499518
dbSNP Id:
rs376699778
ExAC:
12:7360602 C / G
gnomAD v2:
12-7360602-C-G
gnomAD v3:
12-7208006-C-G
gnomAD v4:
12-7208006-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.7208006C>G , CM000674.2:g.7208006C>G | GRCh38 |
| NC_000012.11:g.7360602C>G , CM000674.1:g.7360602C>G | GRCh37 |
| NC_000012.10:g.7251869C>G | NCBI36 |
| NG_008448.1:g.23844C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000675855.1:c.1111-4C>G MANE Select | ENSP00000502374.1:n.1111-4C>G | |
| ENST00000266563.9:c.1000-4C>G | ENSP00000266563.5:n.1000-4C>G | |
| ENST00000266564.7:c.1087-4C>G | ENSP00000266564.3:n.1087-4C>G | |
| ENST00000396637.7:c.1021-4C>G | ENSP00000379877.3:n.1021-4C>G | |
| ENST00000412720.6:c.1174-4C>G | ENSP00000391601.2:n.1174-4C>G | |
| ENST00000420616.6:c.1111-4C>G | ENSP00000410159.2:n.1111-4C>G | |
| ENST00000434354.6:c.1156-4C>G | ENSP00000407401.2:n.1156-4C>G | |
| ENST00000455147.6:c.1111-4C>G | ENSP00000400647.2:n.1111-4C>G | |
| NM_000319.4:c.1087-4C>G | NP_000310.2:n.1087-4C>G | |
| NM_001131023.1:c.1156-4C>G | NP_001124495.1:n.1156-4C>G | |
| NM_001131024.1:c.1000-4C>G | NP_001124496.1:n.1000-4C>G | |
| NM_001131025.1:c.1111-4C>G | NP_001124497.1:n.1111-4C>G | |
| NM_001131026.1:c.1111-4C>G | NP_001124498.1:n.1111-4C>G | |
| NM_001300789.1:c.1174-4C>G | NP_001287718.1:n.1174-4C>G | |
| XM_005253455.1:c.1063-4C>G | XP_005253512.1:n.1063-4C>G | |
| XM_011520793.1:c.1219-4C>G | XP_011519095.1:n.1219-4C>G | |
| XM_011520794.1:c.1219-4C>G | XP_011519096.1:n.1219-4C>G | |
| XM_011520795.1:c.1156-4C>G | XP_011519097.1:n.1156-4C>G | |
| XM_011520796.1:c.1156-4C>G | XP_011519098.1:n.1156-4C>G | |
| XM_011520797.1:c.1111-4C>G | XP_011519099.1:n.1111-4C>G | |
| XM_011520798.1:c.1111-4C>G | XP_011519100.1:n.1111-4C>G | |
| XM_011520799.1:c.1111-4C>G | XP_011519101.1:n.1111-4C>G | |
| XM_011520800.1:c.1111-4C>G | XP_011519102.1:n.1111-4C>G | |
| XM_011520801.1:c.1108-4C>G | XP_011519103.1:n.1108-4C>G | |
| XM_011520802.1:c.862-4C>G | XP_011519104.1:n.862-4C>G | |
| NM_001351124.1:c.1000-4C>G | NP_001338053.1:n.1000-4C>G | |
| NM_001351126.1:c.1000-4C>G | NP_001338055.1:n.1000-4C>G | |
| NM_001351127.1:c.1000-4C>G | NP_001338056.1:n.1000-4C>G | |
| NM_001351128.1:c.1000-4C>G | NP_001338057.1:n.1000-4C>G | |
| NM_001351130.1:c.1000-4C>G | NP_001338059.1:n.1000-4C>G | |
| NM_001351131.1:c.1111-4C>G | NP_001338060.1:n.1111-4C>G | |
| NM_001351132.1:c.1111-4C>G | NP_001338061.1:n.1111-4C>G | |
| NM_001351133.1:c.1111-4C>G | NP_001338062.1:n.1111-4C>G | |
| NM_001351134.1:c.1111-4C>G | NP_001338063.1:n.1111-4C>G | |
| NM_001351135.1:c.1108-4C>G | NP_001338064.1:n.1108-4C>G | |
| NM_001351136.1:c.1102-4C>G | NP_001338065.1:n.1102-4C>G | |
| NM_001351137.1:c.1063-4C>G | NP_001338066.1:n.1063-4C>G | |
| NM_001351138.1:c.1045-4C>G | NP_001338067.1:n.1045-4C>G | |
| NM_001351139.1:c.976-4C>G | NP_001338068.1:n.976-4C>G | |
| NM_001351140.1:c.976-4C>G | NP_001338069.1:n.976-4C>G | |
| XM_011520793.2:c.1219-4C>G | XP_011519095.1:n.1219-4C>G | |
| XM_011520802.2:c.862-4C>G | XP_011519104.1:n.862-4C>G | |
| XM_017019744.1:c.1555-4C>G | XP_016875233.1:n.1555-4C>G | |
| XM_017019745.1:c.1555-4C>G | XP_016875234.1:n.1555-4C>G | |
| XM_017019746.1:c.1444-4C>G | XP_016875235.1:n.1444-4C>G | |
| XM_017019747.1:c.1420-4C>G | XP_016875236.1:n.1420-4C>G | |
| XM_017019748.1:c.1156-4C>G | XP_016875237.1:n.1156-4C>G | |
| XM_017019749.1:c.1111-4C>G | XP_016875238.1:n.1111-4C>G | |
| XM_017019750.1:c.1087-4C>G | XP_016875239.1:n.1087-4C>G | |
| XR_001748833.1:n.1597-4C>G | ||
| NM_000319.5:c.1087-4C>G | NP_000310.2:n.1087-4C>G | |
| NM_001131023.2:c.1156-4C>G | NP_001124495.1:n.1156-4C>G | |
| NM_001131024.2:c.1000-4C>G | NP_001124496.1:n.1000-4C>G | |
| NM_001131025.2:c.1111-4C>G | NP_001124497.1:n.1111-4C>G | |
| NM_001131026.2:c.1111-4C>G | NP_001124498.1:n.1111-4C>G | |
| NM_001300789.3:c.1111-4C>G | NP_001287718.2:n.1111-4C>G | |
| NM_001351124.3:c.1000-4C>G | NP_001338053.1:n.1000-4C>G | |
| NM_001351126.2:c.1000-4C>G | NP_001338055.1:n.1000-4C>G | |
| NM_001351127.2:c.1000-4C>G | NP_001338056.1:n.1000-4C>G | |
| NM_001351128.2:c.1000-4C>G | NP_001338057.1:n.1000-4C>G | |
| NM_001351130.3:c.1000-4C>G | NP_001338059.1:n.1000-4C>G | |
| NM_001351131.2:c.1111-4C>G | NP_001338060.1:n.1111-4C>G | |
| NM_001351132.2:c.1111-4C>G MANE Select | NP_001338061.1:n.1111-4C>G | |
| NM_001351133.2:c.1111-4C>G | NP_001338062.1:n.1111-4C>G | |
| NM_001351134.2:c.1111-4C>G | NP_001338063.1:n.1111-4C>G | |
| NM_001351135.3:c.1045-4C>G | NP_001338064.2:n.1045-4C>G | |
| NM_001351136.2:c.1102-4C>G | NP_001338065.1:n.1102-4C>G | |
| NM_001351137.3:c.1000-4C>G | NP_001338066.2:n.1000-4C>G | |
| NM_001351138.2:c.1045-4C>G | NP_001338067.1:n.1045-4C>G | |
| NM_001351139.2:c.976-4C>G | NP_001338068.1:n.976-4C>G | |
| NM_001351140.2:c.976-4C>G | NP_001338069.1:n.976-4C>G | |
| NM_001374645.1:c.1000-4C>G | NP_001361574.1:n.1000-4C>G | |
| NM_001374646.1:c.1000-4C>G | NP_001361575.1:n.1000-4C>G | |
| NM_001374647.2:c.1111-4C>G | NP_001361576.1:n.1111-4C>G | |
| NM_001374648.2:c.1000-4C>G | NP_001361577.1:n.1000-4C>G | |
| NM_001374649.2:c.976-4C>G | NP_001361578.1:n.976-4C>G |