Linked Data
ClinVar Variation Id:
1642880
ClinVar RCV Id:
RCV002145719
dbSNP Id:
rs367992906
ExAC:
1:11855295 A / G
gnomAD v2:
1-11855295-A-G
gnomAD v4:
1-11795238-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11795238A>G , CM000663.2:g.11795238A>G | GRCh38 |
| NC_000001.10:g.11855295A>G , CM000663.1:g.11855295A>G | GRCh37 |
| NC_000001.9:g.11777882A>G | NCBI36 |
| NG_013351.1:g.15866T>C , LRG_726:g.15866T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376585.6:c.1014T>C | ENSP00000365770.1:p.Tyr338= | |
| ENST00000376590.9:c.891T>C MANE Select | ENSP00000365775.3:p.Tyr297= | |
| ENST00000376592.6:c.891T>C | ENSP00000365777.1:p.Tyr297= | |
| ENST00000423400.7:c.1011T>C | ENSP00000398908.3:p.Tyr337= | |
| ENST00000641407.1:c.891T>C | ENSP00000493098.1:p.Tyr297= | |
| ENST00000641446.1:c.891T>C | ENSP00000493262.1:p.Tyr297= | |
| ENST00000641721.1:n.754T>C | ||
| ENST00000641747.1:c.*403T>C | ENSP00000493116.1:n.*403T>C | |
| ENST00000641759.1:n.1026T>C | ||
| ENST00000641805.1:n.1174T>C | ||
| ENST00000641820.1:c.156T>C | ENSP00000492937.1:p.Tyr52= | |
| ENST00000376583.7:c.1014T>C | ENSP00000365767.3:p.Tyr338= | |
| ENST00000376585.5:c.1014T>C | ENSP00000365770.1:p.Tyr338= | |
| ENST00000376590.7:c.891T>C | ENSP00000365775.3:p.Tyr297= | |
| ENST00000376592.5:c.891T>C | ENSP00000365777.1:p.Tyr297= | |
| NM_005957.4:c.891T>C , LRG_726t1:c.891T>C | NP_005948.3:p.Tyr297= | |
| XM_005263458.2:c.1014T>C | XP_005263515.1:p.Tyr338= | |
| XM_005263460.3:c.891T>C | XP_005263517.1:p.Tyr297= | |
| XM_005263461.3:c.891T>C | XP_005263518.1:p.Tyr297= | |
| XM_005263462.3:c.891T>C | XP_005263519.1:p.Tyr297= | |
| XM_005263463.2:c.645T>C | XP_005263520.1:p.Tyr215= | |
| XM_011541495.1:c.1011T>C | XP_011539797.1:p.Tyr337= | |
| XM_011541496.1:c.1014T>C | XP_011539798.1:p.Tyr338= | |
| NM_001330358.1:c.1014T>C | NP_001317287.1:p.Tyr338= | |
| XM_005263460.5:c.891T>C | XP_005263517.1:p.Tyr297= | |
| XM_005263462.4:c.891T>C | XP_005263519.1:p.Tyr297= | |
| XM_005263463.4:c.645T>C | XP_005263520.1:p.Tyr215= | |
| XM_011541495.3:c.1011T>C | XP_011539797.1:p.Tyr337= | |
| XM_011541496.3:c.1014T>C | XP_011539798.1:p.Tyr338= | |
| XM_017001328.2:c.1014T>C | XP_016856817.1:p.Tyr338= | |
| XM_024447198.1:c.645T>C | XP_024302966.1:p.Tyr215= | |
| XR_002956640.1:n.1758T>C | ||
| NM_005957.5:c.891T>C MANE Select | NP_005948.3:p.Tyr297= | |
| NM_001330358.2:c.1014T>C | NP_001317287.1:p.Tyr338= |