Linked Data
ClinVar Variation Id:
317408
dbSNP Id:
rs201676342
ExAC:
15:91337448 A / G
gnomAD v2:
15-91337448-A-G
gnomAD v3:
15-90794218-A-G
gnomAD v4:
15-90794218-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.90794218A>G , CM000677.2:g.90794218A>G | GRCh38 |
| NC_000015.9:g.91337448A>G , CM000677.1:g.91337448A>G | GRCh37 |
| NC_000015.8:g.89138452A>G | NCBI36 |
| NG_007272.1:g.81847A>G , LRG_20:g.81847A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355112.8:c.3071A>G MANE Select | ENSP00000347232.3:p.Tyr1024Cys | |
| ENST00000560559.2:n.1644A>G | ||
| ENST00000648453.1:c.3071A>G | ENSP00000497646.1:p.Tyr1024Cys | |
| ENST00000680772.1:c.3071A>G | ENSP00000506117.1:p.Tyr1024Cys | |
| ENST00000681142.1:c.3071A>G | ENSP00000506682.1:p.Tyr1024Cys | |
| ENST00000355112.7:c.3071A>G | ENSP00000347232.3:p.Tyr1024Cys | |
| ENST00000558825.5:n.418A>G | ||
| ENST00000559724.5:c.*1995A>G | ENSP00000453359.1:n.*1995A>G | |
| ENST00000560136.5:n.1097A>G | ||
| ENST00000560509.5:c.3071A>G | ENSP00000454158.1:p.Tyr1024Cys | |
| ENST00000560559.1:n.608A>G | ||
| NM_000057.3:c.3071A>G | NP_000048.1:p.Tyr1024Cys | |
| NM_001287246.1:c.3071A>G | NP_001274175.1:p.Tyr1024Cys | |
| NM_001287247.1:c.3071A>G | NP_001274176.1:p.Tyr1024Cys | |
| NM_001287248.1:c.1946A>G | NP_001274177.1:p.Tyr649Cys | |
| XM_006720632.2:c.1109A>G | XP_006720695.1:p.Tyr370Cys | |
| XM_011521881.1:c.1757A>G | XP_011520183.1:p.Tyr586Cys | |
| XM_011521881.2:c.1757A>G | XP_011520183.1:p.Tyr586Cys | |
| NM_000057.4:c.3071A>G MANE Select | NP_000048.1:p.Tyr1024Cys | |
| NM_001287246.2:c.3071A>G | NP_001274175.1:p.Tyr1024Cys | |
| NM_001287247.2:c.3071A>G | NP_001274176.1:p.Tyr1024Cys | |
| NM_001287248.2:c.1946A>G | NP_001274177.1:p.Tyr649Cys |