Linked Data
ClinVar Variation Id:
432005
dbSNP Id:
rs563666662
gnomAD v4:
11-22270368-A-G
COSMIC:
COSM390444
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22270368A>G , CM000673.2:g.22270368A>G | GRCh38 |
| NC_000011.9:g.22291914A>G , CM000673.1:g.22291914A>G | GRCh37 |
| NC_000011.8:g.22248490A>G | NCBI36 |
| NG_015844.1:g.82193A>G , LRG_868:g.82193A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682266.1:c.1505A>G | ENSP00000507766.1:p.Tyr502Cys | |
| ENST00000682341.1:c.1913A>G | ENSP00000508251.1:p.Tyr638Cys | |
| ENST00000683197.1:c.1913A>G | ENSP00000507641.1:p.Tyr638Cys | |
| ENST00000683411.1:c.1505A>G | ENSP00000508397.1:p.Tyr502Cys | |
| ENST00000683437.1:c.1505A>G | ENSP00000508408.1:p.Tyr502Cys | |
| ENST00000683613.1:n.2949A>G | ||
| ENST00000684663.1:c.1910A>G | ENSP00000508009.1:p.Tyr637Cys | |
| ENST00000324559.9:c.1955A>G MANE Select | ENSP00000315371.9:p.Tyr652Cys | |
| ENST00000648804.1:n.2290A>G | ||
| ENST00000324559.8:c.1955A>G | ENSP00000315371.8:p.Tyr652Cys | |
| NM_001142649.1:c.1952A>G | NP_001136121.1:p.Tyr651Cys | |
| NM_213599.2:c.1955A>G , LRG_868t1:c.1955A>G | NP_998764.1:p.Tyr652Cys | |
| XM_005252820.2:c.1913A>G | XP_005252877.2:p.Tyr638Cys | |
| XM_005252821.2:c.1910A>G | XP_005252878.2:p.Tyr637Cys | |
| XM_005252822.3:c.1877A>G | XP_005252879.1:p.Tyr626Cys | |
| XM_005252823.3:c.1874A>G | XP_005252880.1:p.Tyr625Cys | |
| XM_011519949.1:c.1862A>G | XP_011518251.1:p.Tyr621Cys | |
| XM_005252820.3:c.1913A>G | XP_005252877.2:p.Tyr638Cys | |
| XM_005252821.3:c.1910A>G | XP_005252878.2:p.Tyr637Cys | |
| XM_005252822.4:c.1877A>G | XP_005252879.1:p.Tyr626Cys | |
| XM_011519949.2:c.1862A>G | XP_011518251.1:p.Tyr621Cys | |
| NM_001142649.2:c.1952A>G | NP_001136121.1:p.Tyr651Cys | |
| NM_213599.3:c.1955A>G MANE Select | NP_998764.1:p.Tyr652Cys |