Linked Data
ClinVar Variation Id:
301330
dbSNP Id:
rs45578532
gnomAD v2:
10-88428368-G-A
gnomAD v3:
10-86668611-G-A
gnomAD v4:
10-86668611-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.86668611G>A , CM000672.2:g.86668611G>A | GRCh38 |
| NC_000010.10:g.88428368G>A , CM000672.1:g.88428368G>A | GRCh37 |
| NC_000010.9:g.88418348G>A | NCBI36 |
| NG_008876.1:g.5048G>A , LRG_385:g.5048G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000443292.2:c.1487-58G>A | ENSP00000393132.2:n.1487-58G>A | |
| ENST00000685347.1:n.1449-58G>A | ||
| ENST00000686051.1:n.60+41G>A | ||
| ENST00000686176.1:n.60+41G>A | ||
| ENST00000687856.1:c.-23-58G>A | ENSP00000510221.1:n.-23-58G>A | |
| ENST00000688001.1:c.-23-58G>A | ENSP00000508987.1:n.-23-58G>A | |
| ENST00000688678.1:c.-24+41G>A | ENSP00000510048.1:n.-24+41G>A | |
| ENST00000688785.1:c.-23-58G>A | ENSP00000509572.1:n.-23-58G>A | |
| ENST00000689740.1:c.-22+41G>A | ENSP00000510300.1:n.-22+41G>A | |
| ENST00000691462.1:c.-23-58G>A | ENSP00000509930.1:n.-23-58G>A | |
| ENST00000691495.1:n.60+41G>A | ||
| ENST00000692941.1:n.2070-58G>A | ||
| ENST00000693680.1:c.-81G>A | ENSP00000509539.1:n.-81G>A | |
| ENST00000263066.11:c.-24+41G>A MANE Plus Clinical | ENSP00000263066.7:n.-24+41G>A | |
| ENST00000361373.9:c.-24+41G>A MANE Select | ENSP00000355296.3:n.-24+41G>A | |
| ENST00000429277.7:c.-24+41G>A | ENSP00000401437.3:n.-24+41G>A | |
| ENST00000623056.4:c.-22+41G>A | ENSP00000485500.1:n.-22+41G>A | |
| ENST00000429277.6:c.-24+41G>A | ENSP00000401437.2:n.-24+41G>A | |
| ENST00000623056.3:c.-22+36G>A | ENSP00000485500.1:n.-22+36G>A | |
| NM_001080116.1:c.-81G>A , LRG_385t2:c.-81G>A | NP_001073585.1:n.-81G>A | |
| NM_001171610.1:c.-24+41G>A | NP_001165081.1:n.-24+41G>A | |
| XM_005269464.3:c.-24+41G>A | XP_005269521.1:n.-24+41G>A | |
| XM_005269466.3:c.-24+41G>A | XP_005269523.1:n.-24+41G>A | |
| XM_005269468.3:c.-24+41G>A | XP_005269525.1:n.-24+41G>A | |
| XM_011539184.1:c.-24+41G>A | XP_011537486.1:n.-24+41G>A | |
| XM_011539185.1:c.-23-58G>A | XP_011537487.1:n.-23-58G>A | |
| XM_011539186.1:c.-24+41G>A | XP_011537488.1:n.-24+41G>A | |
| XM_011539187.1:c.-24+41G>A | XP_011537489.1:n.-24+41G>A | |
| XM_011539188.1:c.-24+41G>A | XP_011537490.1:n.-24+41G>A | |
| XM_011539189.1:c.-23-58G>A | XP_011537491.1:n.-23-58G>A | |
| XM_011539191.1:c.-24+41G>A | XP_011537493.1:n.-24+41G>A | |
| XM_011539192.1:c.-24+41G>A | XP_011537494.1:n.-24+41G>A | |
| XM_011539193.1:c.-495-58G>A | XP_011537495.1:n.-495-58G>A | |
| XM_011539194.1:c.-495-58G>A | XP_011537496.1:n.-495-58G>A | |
| XM_011539195.1:c.-24+41G>A | XP_011537497.1:n.-24+41G>A | |
| XM_005269464.4:c.-24+41G>A | XP_005269521.1:n.-24+41G>A | |
| XM_005269466.4:c.-24+41G>A | XP_005269523.1:n.-24+41G>A | |
| XM_005269468.4:c.-24+41G>A | XP_005269525.1:n.-24+41G>A | |
| XM_011539184.2:c.-24+41G>A | XP_011537486.1:n.-24+41G>A | |
| XM_011539185.2:c.-23-58G>A | XP_011537487.1:n.-23-58G>A | |
| XM_011539186.2:c.-24+41G>A | XP_011537488.1:n.-24+41G>A | |
| XM_011539187.2:c.-24+41G>A | XP_011537489.1:n.-24+41G>A | |
| XM_011539188.2:c.-24+41G>A | XP_011537490.1:n.-24+41G>A | |
| XM_011539190.2:c.-24+41G>A | XP_011537492.1:n.-24+41G>A | |
| XM_011539191.2:c.-24+41G>A | XP_011537493.1:n.-24+41G>A | |
| XM_011539195.2:c.-24+41G>A | XP_011537497.1:n.-24+41G>A | |
| XM_017015606.1:c.-23-58G>A | XP_016871095.1:n.-23-58G>A | |
| XM_017015608.1:c.-23-58G>A | XP_016871097.1:n.-23-58G>A | |
| XM_017015609.1:c.-23-58G>A | XP_016871098.1:n.-23-58G>A | |
| XM_024447785.1:c.-24+41G>A | XP_024303553.1:n.-24+41G>A | |
| XM_024447786.1:c.-24+41G>A | XP_024303554.1:n.-24+41G>A | |
| XM_024447787.1:c.-24+41G>A | XP_024303555.1:n.-24+41G>A | |
| NM_001080114.2:c.-24+41G>A | NP_001073583.1:n.-24+41G>A | |
| NM_001080115.2:c.-24+41G>A | NP_001073584.1:n.-24+41G>A | |
| NM_001171610.2:c.-24+41G>A | NP_001165081.1:n.-24+41G>A | |
| NM_001171611.2:c.-24+41G>A | NP_001165082.1:n.-24+41G>A | |
| NM_001368063.1:c.-23-58G>A | NP_001354992.1:n.-23-58G>A | |
| NM_001368064.1:c.-23-58G>A | NP_001354993.1:n.-23-58G>A | |
| NM_001368065.1:c.-24+41G>A | NP_001354994.1:n.-24+41G>A | |
| NM_001368066.1:c.-24+41G>A | NP_001354995.1:n.-24+41G>A | |
| NM_001368067.1:c.-24+41G>A MANE Plus Clinical | NP_001354996.1:n.-24+41G>A | |
| NM_001368068.1:c.-23-58G>A | NP_001354997.1:n.-23-58G>A | |
| NM_007078.3:c.-24+41G>A MANE Select | NP_009009.1:n.-24+41G>A |