Linked Data
ClinVar Variation Id:
536463
dbSNP Id:
rs145253993
ExAC:
15:55527116 T / C
gnomAD v2:
15-55527116-T-C
gnomAD v3:
15-55234918-T-C
gnomAD v4:
15-55234918-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.55234918T>C , CM000677.2:g.55234918T>C | GRCh38 |
| NC_000015.9:g.55527116T>C , CM000677.1:g.55527116T>C | GRCh37 |
| NC_000015.8:g.53314408T>C | NCBI36 |
| NG_009103.1:g.59886A>G , LRG_96:g.59886A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000697641.1:n.2053A>G | ||
| ENST00000697642.1:c.17A>G | ENSP00000513368.1:p.Tyr6Cys | |
| ENST00000697643.1:c.17A>G | ENSP00000513369.1:p.Tyr6Cys | |
| ENST00000336787.6:c.17A>G MANE Select | ENSP00000337761.1:p.Tyr6Cys | |
| ENST00000336787.5:c.17A>G | ENSP00000337761.1:p.Tyr6Cys | |
| ENST00000396307.6:c.17A>G | ENSP00000379601.2:p.Tyr6Cys | |
| ENST00000563262.5:c.17A>G | ENSP00000457595.1:p.Tyr6Cys | |
| ENST00000564609.5:c.17A>G | ENSP00000455012.1:p.Tyr6Cys | |
| ENST00000565972.5:c.17A>G | ENSP00000456536.1:p.Tyr6Cys | |
| ENST00000566877.5:c.17A>G | ENSP00000454695.1:p.Tyr6Cys | |
| ENST00000567380.5:c.17A>G | ENSP00000458127.1:p.Tyr6Cys | |
| ENST00000568803.1:c.17A>G | ENSP00000457517.1:p.Tyr6Cys | |
| ENST00000569493.5:c.17A>G | ENSP00000456059.1:p.Tyr6Cys | |
| NM_004580.4:c.17A>G | NP_004571.2:p.Tyr6Cys | |
| NM_183234.2:c.17A>G | NP_899057.1:p.Tyr6Cys | |
| NM_183235.2:c.17A>G | NP_899058.1:p.Tyr6Cys | |
| NM_183236.2:c.17A>G | NP_899059.1:p.Tyr6Cys | |
| XM_005254576.3:c.17A>G | XP_005254633.1:p.Tyr6Cys | |
| XM_011521852.1:c.17A>G | XP_011520154.1:p.Tyr6Cys | |
| XM_011521853.1:c.17A>G | XP_011520155.1:p.Tyr6Cys | |
| XM_011521854.1:c.17A>G | XP_011520156.1:p.Tyr6Cys | |
| XM_011521855.1:c.17A>G | XP_011520157.1:p.Tyr6Cys | |
| XM_011521856.1:c.17A>G | XP_011520158.1:p.Tyr6Cys | |
| XM_005254576.5:c.17A>G | XP_005254633.1:p.Tyr6Cys | |
| XM_011521855.3:c.17A>G | XP_011520157.1:p.Tyr6Cys | |
| XM_011521856.2:c.17A>G | XP_011520158.1:p.Tyr6Cys | |
| XM_024450009.1:c.17A>G | XP_024305777.1:p.Tyr6Cys | |
| NM_183235.3:c.17A>G MANE Select | NP_899058.1:p.Tyr6Cys | |
| NM_004580.5:c.17A>G | NP_004571.2:p.Tyr6Cys | |
| NM_183236.3:c.17A>G | NP_899059.1:p.Tyr6Cys |