Linked Data
ClinVar Variation Id:
185585
dbSNP Id:
rs757498880
ExAC:
10:89711909 A / G
gnomAD v2:
10-89711909-A-G
gnomAD v3:
10-87952152-A-G
gnomAD v4:
10-87952152-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87952152A>G , CM000672.2:g.87952152A>G | GRCh38 |
| NC_000010.10:g.89711909A>G , CM000672.1:g.89711909A>G | GRCh37 |
| NC_000010.9:g.89701889A>G | NCBI36 |
| NG_007466.2:g.93714A>G , LRG_311:g.93714A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.527A>G | ENSP00000514759.2:p.Tyr176Cys | |
| ENST00000710265.1:c.527A>G | ENSP00000518161.1:p.Tyr176Cys | |
| ENST00000472832.3:c.527A>G | ENSP00000483066.2:p.Tyr176Cys | |
| ENST00000688158.2:n.1262A>G | ||
| ENST00000688922.2:c.*357A>G | ENSP00000508742.2:n.*357A>G | |
| ENST00000700021.1:c.482A>G | ENSP00000514757.1:p.Tyr161Cys | |
| ENST00000700022.1:c.493-5701A>G | ENSP00000514758.1:n.493-5701A>G | |
| ENST00000700023.1:n.1685A>G | ||
| ENST00000700024.1:n.1919A>G | ||
| ENST00000700025.1:n.1296A>G | ||
| ENST00000700029.1:c.361A>G | ||
| ENST00000706954.1:c.527A>G | ENSP00000516674.1:p.Tyr176Cys | |
| ENST00000706955.1:c.*562A>G | ENSP00000516675.1:n.*562A>G | |
| ENST00000686459.1:c.*113A>G | ENSP00000508909.1:n.*113A>G | |
| ENST00000688158.1:c.*638A>G | ENSP00000509254.1:n.*638A>G | |
| ENST00000688308.1:c.527A>G | ENSP00000508752.1:p.Tyr176Cys | |
| ENST00000688922.1:c.448A>G | ||
| ENST00000693560.1:c.1046A>G | ENSP00000509861.1:p.Tyr349Cys | |
| ENST00000371953.8:c.527A>G MANE Select | ENSP00000361021.3:p.Tyr176Cys | |
| ENST00000371953.7:c.527A>G | ENSP00000361021.3:p.Tyr176Cys | |
| NM_000314.5:c.527A>G | NP_000305.3:p.Tyr176Cys | |
| NM_000314.6:c.527A>G | NP_000305.3:p.Tyr176Cys | |
| NM_001304717.2:c.1046A>G | NP_001291646.2:p.Tyr349Cys | |
| NM_001304718.1:c.-65A>G | NP_001291647.1:n.-65A>G | |
| XM_006717926.2:c.482A>G | XP_006717989.1:p.Tyr161Cys | |
| XM_011539981.1:c.527A>G | XP_011538283.1:p.Tyr176Cys | |
| XM_011539982.1:c.431A>G | XP_011538284.1:p.Tyr144Cys | |
| XR_945789.1:n.1398A>G | ||
| XR_945790.1:n.1515A>G | ||
| XR_945791.1:n.1205-5701A>G | ||
| NM_000314.7:c.527A>G | NP_000305.3:p.Tyr176Cys | |
| NM_001304717.5:c.1046A>G | NP_001291646.4:p.Tyr349Cys | |
| NM_001304718.2:c.-65A>G | NP_001291647.1:n.-65A>G | |
| NM_000314.8:c.527A>G MANE Select | NP_000305.3:p.Tyr176Cys |