Linked Data
ClinVar Variation Id:
142713
dbSNP Id:
rs368466538
gnomAD v2:
19-1226569-C-G
gnomAD v3:
19-1226570-C-G
gnomAD v4:
19-1226570-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1226570C>G , CM000681.2:g.1226570C>G | GRCh38 |
| NC_000019.9:g.1226569C>G , CM000681.1:g.1226569C>G | GRCh37 |
| NC_000019.8:g.1177569C>G | NCBI36 |
| NG_007460.2:g.42164C>G , LRG_319:g.42164C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.*2826C>G | ENSP00000490268.2:n.*2826C>G | |
| ENST00000585748.3:c.853C>G | ENSP00000477641.2:p.Arg285Gly | |
| ENST00000585851.2:c.1051C>G | ENSP00000467912.2:p.Arg351Gly | |
| ENST00000326873.12:c.1225C>G MANE Select | ENSP00000324856.6:p.Arg409Gly | |
| ENST00000326873.11:c.1225C>G | ENSP00000324856.6:p.Arg409Gly | |
| ENST00000585465.2:n.2958C>G | ||
| ENST00000586243.5:c.1224C>G | ENSP00000467240.2:p.Ala408= | |
| ENST00000589152.5:n.1923C>G | ||
| NM_000455.4:c.1225C>G , LRG_319t1:c.1225C>G | NP_000446.1:p.Arg409Gly | |
| XM_005259617.1:c.1220C>G | XP_005259674.1:p.Pro407Arg | |
| XM_011528209.1:c.998C>G | XP_011526511.1:p.Pro333Arg | |
| XM_005259617.3:c.1220C>G | XP_005259674.1:p.Pro407Arg | |
| XM_011528209.2:c.998C>G | XP_011526511.1:p.Pro333Arg | |
| XR_001753738.2:n.2031C>G | ||
| XR_001753740.2:n.2001C>G | ||
| NM_000455.5:c.1225C>G MANE Select | NP_000446.1:p.Arg409Gly |