Linked Data
ClinVar Variation Id:
374881
dbSNP Id:
rs759218713
ExAC:
1:29522747 T / C
gnomAD v2:
1-29522747-T-C
gnomAD v3:
1-29196235-T-C
gnomAD v4:
1-29196235-T-C
PubMed:
PMID:27817865
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.29196235T>C , CM000663.2:g.29196235T>C | GRCh38 |
| NC_000001.10:g.29522747T>C , CM000663.1:g.29522747T>C | GRCh37 |
| NC_000001.9:g.29395334T>C | NCBI36 |
| NG_053058.1:g.39724A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000263702.11:c.854A>G MANE Select | ENSP00000263702.6:p.Tyr285Cys | |
| ENST00000263702.10:c.854A>G | ENSP00000263702.6:p.Tyr285Cys | |
| ENST00000373791.7:c.626A>G | ENSP00000362896.3:p.Tyr209Cys | |
| ENST00000453185.5:n.516A>G | ||
| ENST00000463412.1:c.473A>G | ENSP00000436831.1:p.Tyr158Cys | |
| ENST00000473030.5:n.503A>G | ||
| ENST00000475773.5:n.272A>G | ||
| ENST00000478505.6:n.753A>G | ||
| ENST00000483435.5:n.98A>G | ||
| ENST00000490529.5:n.739A>G | ||
| NM_001024732.2:c.626A>G | NP_001019903.2:p.Tyr209Cys | |
| NM_016011.3:c.854A>G | NP_057095.3:p.Tyr285Cys | |
| XM_005245885.1:c.938A>G | XP_005245942.1:p.Tyr313Cys | |
| XM_005245887.1:c.626A>G | XP_005245944.1:p.Tyr209Cys | |
| XM_011541539.1:c.1083A>G | XP_011539841.1:p.Leu361= | |
| XM_011541540.1:c.999A>G | XP_011539842.1:p.Leu333= | |
| XM_011541541.1:c.938A>G | XP_011539843.1:p.Tyr313Cys | |
| XM_011541542.1:c.771A>G | XP_011539844.1:p.Leu257= | |
| XM_011541543.1:c.771A>G | XP_011539845.1:p.Leu257= | |
| XM_011541544.1:c.771A>G | XP_011539846.1:p.Leu257= | |
| XM_011541545.1:c.771A>G | XP_011539847.1:p.Leu257= | |
| XM_011541546.1:c.771A>G | XP_011539848.1:p.Leu257= | |
| XM_011541547.1:c.771A>G | XP_011539849.1:p.Leu257= | |
| XM_011541548.1:c.771A>G | XP_011539850.1:p.Leu257= | |
| XM_011541549.1:c.771A>G | XP_011539851.1:p.Leu257= | |
| XM_011541550.1:c.771A>G | XP_011539852.1:p.Leu257= | |
| XM_011541551.1:c.771A>G | XP_011539853.1:p.Leu257= | |
| XM_011541552.1:c.771A>G | XP_011539854.1:p.Leu257= | |
| XM_011541553.1:c.771A>G | XP_011539855.1:p.Leu257= | |
| XM_011541554.1:c.771A>G | XP_011539856.1:p.Leu257= | |
| XR_946662.1:n.1101A>G | ||
| XR_946663.1:n.1101A>G | ||
| XR_946664.1:n.853A>G | ||
| NM_001024732.3:c.626A>G | NP_001019903.3:p.Tyr209Cys | |
| NM_001349711.1:c.626A>G | NP_001336640.1:p.Tyr209Cys | |
| NM_001349712.1:c.626A>G | NP_001336641.1:p.Tyr209Cys | |
| NM_001349713.1:c.626A>G | NP_001336642.1:p.Tyr209Cys | |
| NM_001349714.1:c.626A>G | NP_001336643.1:p.Tyr209Cys | |
| NM_001349715.1:c.959A>G | NP_001336644.1:p.Tyr320Cys | |
| NM_001349716.1:c.938A>G | NP_001336645.1:p.Tyr313Cys | |
| NM_001349717.1:c.704A>G | NP_001336646.1:p.Tyr235Cys | |
| NM_016011.4:c.854A>G | NP_057095.4:p.Tyr285Cys | |
| NR_146212.1:n.1139A>G | ||
| NR_146213.1:n.906A>G | ||
| NR_146214.1:n.1159A>G | ||
| NR_146215.1:n.1033A>G | ||
| XM_011541540.2:c.999A>G | XP_011539842.1:p.Leu333= | |
| XM_017001411.1:c.771A>G | XP_016856900.1:p.Leu257= | |
| XM_017001412.1:c.771A>G | XP_016856901.1:p.Leu257= | |
| XM_017001413.1:c.626A>G | XP_016856902.1:p.Tyr209Cys | |
| XM_017001416.1:c.626A>G | XP_016856905.1:p.Tyr209Cys | |
| XM_024447442.1:c.626A>G | XP_024303210.1:p.Tyr209Cys | |
| XM_024447443.1:c.626A>G | XP_024303211.1:p.Tyr209Cys | |
| XM_024447444.1:c.626A>G | XP_024303212.1:p.Tyr209Cys | |
| XM_024447446.1:c.626A>G | XP_024303214.1:p.Tyr209Cys | |
| XM_024447448.1:c.626A>G | XP_024303216.1:p.Tyr209Cys | |
| XM_024447450.1:c.626A>G | XP_024303218.1:p.Tyr209Cys | |
| XM_024447452.1:c.626A>G | XP_024303220.1:p.Tyr209Cys | |
| XR_001737209.1:n.1207A>G | ||
| XR_001737210.1:n.1476A>G | ||
| XR_002956765.1:n.1004A>G | ||
| XR_946663.2:n.1101A>G | ||
| NM_001024732.4:c.626A>G | NP_001019903.3:p.Tyr209Cys | |
| NM_001349711.2:c.626A>G | NP_001336640.1:p.Tyr209Cys | |
| NM_001349712.2:c.626A>G | NP_001336641.1:p.Tyr209Cys | |
| NM_001349713.2:c.626A>G | NP_001336642.1:p.Tyr209Cys | |
| NM_001349714.2:c.626A>G | NP_001336643.1:p.Tyr209Cys | |
| NM_001349715.2:c.959A>G | NP_001336644.1:p.Tyr320Cys | |
| NM_001349716.2:c.938A>G | NP_001336645.1:p.Tyr313Cys | |
| NM_001349717.2:c.704A>G | NP_001336646.1:p.Tyr235Cys | |
| NM_016011.5:c.854A>G MANE Select | NP_057095.4:p.Tyr285Cys | |
| NR_146212.2:n.1115A>G | ||
| NR_146213.2:n.882A>G | ||
| NR_146214.2:n.1135A>G | ||
| NR_146215.2:n.1009A>G |