Linked Data
ClinVar Variation Id:
1772153
ClinVar RCV Id:
RCV002391715
dbSNP Id:
rs1238533173
gnomAD v2:
1-78401673-A-G
gnomAD v3:
1-77935988-A-G
gnomAD v4:
1-77935988-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.77935988A>G , CM000663.2:g.77935988A>G | GRCh38 |
| NC_000001.10:g.78401673A>G , CM000663.1:g.78401673A>G | GRCh37 |
| NC_000001.9:g.78174261A>G | NCBI36 |
| NG_016625.1:g.52474A>G , LRG_442:g.52474A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334785.12:c.1417A>G MANE Select | ENSP00000333938.7:p.Arg473Gly | |
| ENST00000330010.12:c.1225A>G | ENSP00000327363.8:p.Arg409Gly | |
| ENST00000334785.11:c.1417A>G | ENSP00000333938.7:p.Arg473Gly | |
| ENST00000342754.5:c.1116A>G | ||
| ENST00000480732.2:n.991A>G | ||
| NM_001172309.1:c.1225A>G | NP_001165780.1:p.Arg409Gly | |
| NM_144573.3:c.1417A>G , LRG_442t1:c.1417A>G | NP_653174.3:p.Arg473Gly | |
| XM_005271322.2:c.1417A>G | XP_005271379.1:p.Arg473Gly | |
| XM_005271323.2:c.1375A>G | XP_005271380.1:p.Arg459Gly | |
| XM_005271324.3:c.1225A>G | XP_005271381.1:p.Arg409Gly | |
| XM_005271325.2:c.1251+2509A>G | XP_005271382.1:n.1251+2509A>G | |
| XM_005271326.2:c.1183A>G | XP_005271383.1:p.Arg395Gly | |
| XM_005271327.2:c.1000A>G | XP_005271384.1:p.Arg334Gly | |
| XM_005271322.4:c.1417A>G | XP_005271379.1:p.Arg473Gly | |
| XM_005271323.4:c.1375A>G | XP_005271380.1:p.Arg459Gly | |
| XM_005271324.5:c.1225A>G | XP_005271381.1:p.Arg409Gly | |
| XM_005271325.4:c.1251+2509A>G | XP_005271382.1:n.1251+2509A>G | |
| XM_005271326.4:c.1183A>G | XP_005271383.1:p.Arg395Gly | |
| XM_005271327.4:c.1000A>G | XP_005271384.1:p.Arg334Gly | |
| NM_001172309.2:c.1225A>G | NP_001165780.1:p.Arg409Gly | |
| NM_144573.4:c.1417A>G MANE Select | NP_653174.3:p.Arg473Gly |