Linked Data
ClinVar Variation Id:
1329333
ClinVar RCV Id:
RCV001799376
dbSNP Id:
rs1650735272
gnomAD v4:
1-77936049-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.77936049A>G , CM000663.2:g.77936049A>G | GRCh38 |
| NC_000001.10:g.78401734A>G , CM000663.1:g.78401734A>G | GRCh37 |
| NC_000001.9:g.78174322A>G | NCBI36 |
| NG_016625.1:g.52535A>G , LRG_442:g.52535A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334785.12:c.1473+5A>G MANE Select | ENSP00000333938.7:n.1473+5A>G | |
| ENST00000330010.12:c.1281+5A>G | ENSP00000327363.8:n.1281+5A>G | |
| ENST00000334785.11:c.1473+5A>G | ENSP00000333938.7:n.1473+5A>G | |
| ENST00000342754.5:c.1172+5A>G | ||
| ENST00000480732.2:n.1047+5A>G | ||
| NM_001172309.1:c.1281+5A>G | NP_001165780.1:n.1281+5A>G | |
| NM_144573.3:c.1473+5A>G , LRG_442t1:c.1473+5A>G | NP_653174.3:n.1473+5A>G | |
| XM_005271322.2:c.1473+5A>G | XP_005271379.1:n.1473+5A>G | |
| XM_005271323.2:c.1431+5A>G | XP_005271380.1:n.1431+5A>G | |
| XM_005271324.3:c.1281+5A>G | XP_005271381.1:n.1281+5A>G | |
| XM_005271325.2:c.1251+2570A>G | XP_005271382.1:n.1251+2570A>G | |
| XM_005271326.2:c.1239+5A>G | XP_005271383.1:n.1239+5A>G | |
| XM_005271327.2:c.1056+5A>G | XP_005271384.1:n.1056+5A>G | |
| XM_005271322.4:c.1473+5A>G | XP_005271379.1:n.1473+5A>G | |
| XM_005271323.4:c.1431+5A>G | XP_005271380.1:n.1431+5A>G | |
| XM_005271324.5:c.1281+5A>G | XP_005271381.1:n.1281+5A>G | |
| XM_005271325.4:c.1251+2570A>G | XP_005271382.1:n.1251+2570A>G | |
| XM_005271326.4:c.1239+5A>G | XP_005271383.1:n.1239+5A>G | |
| XM_005271327.4:c.1056+5A>G | XP_005271384.1:n.1056+5A>G | |
| NM_001172309.2:c.1281+5A>G | NP_001165780.1:n.1281+5A>G | |
| NM_144573.4:c.1473+5A>G MANE Select | NP_653174.3:n.1473+5A>G |