Linked Data
dbSNP Id:
rs747331732
ExAC:
1:6534525 T / C
gnomAD v2:
1-6534525-T-C
gnomAD v4:
1-6474465-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.6474465T>C , CM000663.2:g.6474465T>C | GRCh38 |
| NC_000001.10:g.6534525T>C , CM000663.1:g.6534525T>C | GRCh37 |
| NC_000001.9:g.6457112T>C | NCBI36 |
| NG_007978.1:g.50545A>G , LRG_262:g.50545A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340850.10:c.425A>G | ENSP00000344570.5:p.Tyr142Cys | |
| ENST00000377728.8:c.425A>G MANE Select | ENSP00000366957.3:p.Tyr142Cys | |
| ENST00000377740.5:c.425A>G | ENSP00000366969.4:p.Tyr142Cys | |
| ENST00000377748.6:c.599A>G | ENSP00000366977.2:p.Tyr200Cys | |
| ENST00000400913.6:c.425A>G | ENSP00000383704.1:p.Tyr142Cys | |
| ENST00000400915.8:c.536A>G | ENSP00000383706.4:p.Tyr179Cys | |
| ENST00000489097.6:n.901A>G | ||
| ENST00000535355.6:c.632A>G | ENSP00000441445.1:p.Tyr211Cys | |
| ENST00000537245.6:c.536A>G | ENSP00000439625.2:p.Tyr179Cys | |
| ENST00000673471.2:c.722A>G | ENSP00000500749.1:p.Tyr241Cys | |
| ENST00000674790.1:c.*637A>G | ENSP00000502815.1:n.*637A>G | |
| ENST00000675123.1:c.425A>G | ENSP00000502132.1:p.Tyr142Cys | |
| ENST00000675548.1:c.*253A>G | ENSP00000502684.1:n.*253A>G | |
| ENST00000675694.1:c.425A>G | ENSP00000501925.1:p.Tyr142Cys | |
| ENST00000676255.1:c.387A>G | ENSP00000502459.1:n.387A>G | |
| ENST00000340850.9:c.425A>G | ENSP00000344570.5:p.Tyr142Cys | |
| ENST00000377725.5:c.425A>G | ENSP00000366954.1:p.Tyr142Cys | |
| ENST00000377728.7:c.425A>G | ENSP00000366957.3:p.Tyr142Cys | |
| ENST00000377732.5:c.536A>G | ENSP00000366961.1:p.Tyr179Cys | |
| ENST00000377740.4:c.656A>G | ENSP00000366969.3:p.Tyr219Cys | |
| ENST00000377748.5:c.656A>G | ENSP00000366977.1:p.Tyr219Cys | |
| ENST00000400913.5:c.425A>G | ENSP00000383704.1:p.Tyr142Cys | |
| ENST00000400915.7:c.593A>G | ENSP00000383706.3:p.Tyr198Cys | |
| ENST00000489097.5:n.901A>G | ||
| ENST00000535355.5:c.632A>G | ENSP00000441445.1:p.Tyr211Cys | |
| ENST00000537245.5:c.662A>G | ENSP00000439625.1:p.Tyr221Cys | |
| NM_001042663.1:c.593A>G | NP_001036128.1:p.Tyr198Cys | |
| NM_001042664.1:c.425A>G | NP_001036129.1:p.Tyr142Cys | |
| NM_001042665.1:c.425A>G | NP_001036130.1:p.Tyr142Cys | |
| NM_001265592.1:c.662A>G | NP_001252521.1:p.Tyr221Cys | |
| NM_001265593.1:c.632A>G | NP_001252522.1:p.Tyr211Cys | |
| NM_001265594.1:c.425A>G | NP_001252523.1:p.Tyr142Cys | |
| NM_020631.4:c.425A>G | NP_065682.2:p.Tyr142Cys | |
| NM_198681.3:c.656A>G | NP_941374.2:p.Tyr219Cys | |
| NM_001042663.2:c.593A>G | NP_001036128.1:p.Tyr198Cys | |
| NM_001265594.2:c.425A>G | NP_001252523.1:p.Tyr142Cys | |
| NM_020631.5:c.425A>G | NP_065682.2:p.Tyr142Cys | |
| NM_001042663.3:c.536A>G | NP_001036128.2:p.Tyr179Cys | |
| NM_001265592.2:c.536A>G | NP_001252521.2:p.Tyr179Cys | |
| NM_020631.6:c.425A>G MANE Select | NP_065682.2:p.Tyr142Cys | |
| NM_198681.4:c.425A>G | NP_941374.3:p.Tyr142Cys |