Linked Data
dbSNP Id:
rs766276540
ExAC:
1:78407870 G / C
gnomAD v2:
1-78407870-G-C
gnomAD v4:
1-77942185-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.77942185G>C , CM000663.2:g.77942185G>C | GRCh38 |
| NC_000001.10:g.78407870G>C , CM000663.1:g.78407870G>C | GRCh37 |
| NC_000001.9:g.78180458G>C | NCBI36 |
| NG_016625.1:g.58671G>C , LRG_442:g.58671G>C | |
| NG_033243.2:g.41909C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334785.12:c.1636G>C MANE Select | ENSP00000333938.7:p.Glu546Gln | |
| ENST00000330010.12:c.1444G>C | ENSP00000327363.8:p.Glu482Gln | |
| ENST00000334785.11:c.1636G>C | ENSP00000333938.7:p.Glu546Gln | |
| ENST00000342754.5:c.1335G>C | ||
| ENST00000470735.1:n.475G>C | ||
| ENST00000480732.2:n.1210G>C | ||
| NM_001172309.1:c.1444G>C | NP_001165780.1:p.Glu482Gln | |
| NM_144573.3:c.1636G>C , LRG_442t1:c.1636G>C | NP_653174.3:p.Glu546Gln | |
| XM_005271322.2:c.1636G>C | XP_005271379.1:p.Glu546Gln | |
| XM_005271323.2:c.1594G>C | XP_005271380.1:p.Glu532Gln | |
| XM_005271324.3:c.1444G>C | XP_005271381.1:p.Glu482Gln | |
| XM_005271325.2:c.1414G>C | XP_005271382.1:p.Glu472Gln | |
| XM_005271326.2:c.1402G>C | XP_005271383.1:p.Glu468Gln | |
| XM_005271327.2:c.1219G>C | XP_005271384.1:p.Glu407Gln | |
| XM_005271322.4:c.1636G>C | XP_005271379.1:p.Glu546Gln | |
| XM_005271323.4:c.1594G>C | XP_005271380.1:p.Glu532Gln | |
| XM_005271324.5:c.1444G>C | XP_005271381.1:p.Glu482Gln | |
| XM_005271325.4:c.1414G>C | XP_005271382.1:p.Glu472Gln | |
| XM_005271326.4:c.1402G>C | XP_005271383.1:p.Glu468Gln | |
| XM_005271327.4:c.1219G>C | XP_005271384.1:p.Glu407Gln | |
| NM_001172309.2:c.1444G>C | NP_001165780.1:p.Glu482Gln | |
| NM_144573.4:c.1636G>C MANE Select | NP_653174.3:p.Glu546Gln |