Linked Data
ClinVar Variation Id:
1488316
ClinVar RCV Id:
RCV001976975
dbSNP Id:
rs760349455
ExAC:
12:32793247 A / G
gnomAD v2:
12-32793247-A-G
gnomAD v4:
12-32640313-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.32640313A>G , CM000674.2:g.32640313A>G | GRCh38 |
| NC_000012.11:g.32793247A>G , CM000674.1:g.32793247A>G | GRCh37 |
| NC_000012.10:g.32684514A>G | NCBI36 |
| NG_008626.2:g.245785A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000427716.7:c.2081A>G | ENSP00000394487.2:p.Tyr694Cys | |
| ENST00000531134.7:c.2336A>G | ENSP00000431323.1:p.Tyr779Cys | |
| ENST00000583694.2:c.2081A>G | ENSP00000462623.2:p.Tyr694Cys | |
| ENST00000682739.1:c.1802A>G | ENSP00000507616.1:p.Tyr601Cys | |
| ENST00000683182.1:c.893A>G | ENSP00000507831.1:p.Tyr298Cys | |
| ENST00000684033.1:n.879A>G | ||
| ENST00000525053.6:c.2081A>G | ENSP00000433666.2:p.Tyr694Cys | |
| ENST00000531134.6:c.2336A>G | ENSP00000431323.1:p.Tyr779Cys | |
| ENST00000534526.7:c.2492A>G MANE Select | ENSP00000449273.1:p.Tyr831Cys | |
| ENST00000427716.6:c.2081A>G | ENSP00000394487.2:p.Tyr694Cys | |
| ENST00000493087.5:c.*1492A>G | ENSP00000437109.1:n.*1492A>G | |
| ENST00000494977.1:c.1969A>G | ||
| ENST00000525053.5:c.2417A>G | ENSP00000433666.1:p.Tyr806Cys | |
| ENST00000531134.5:c.2336A>G | ENSP00000431323.1:p.Tyr779Cys | |
| ENST00000534526.6:c.2492A>G | ENSP00000449273.1:p.Tyr831Cys | |
| ENST00000546442.5:c.1802A>G | ENSP00000446695.1:p.Tyr601Cys | |
| ENST00000551984.5:c.*1450A>G | ENSP00000449614.1:n.*1450A>G | |
| NM_001304480.1:c.2417A>G | NP_001291409.1:p.Tyr806Cys | |
| NM_001304481.1:c.2336A>G | NP_001291410.1:p.Tyr779Cys | |
| NM_001304484.1:c.1049A>G | NP_001291413.1:p.Tyr350Cys | |
| NM_139241.3:c.2081A>G | NP_640334.2:p.Tyr694Cys | |
| XM_005253304.3:c.2573A>G | XP_005253361.1:p.Tyr858Cys | |
| XM_005253307.2:c.1802A>G | XP_005253364.1:p.Tyr601Cys | |
| XM_005253308.3:c.1802A>G | XP_005253365.1:p.Tyr601Cys | |
| XM_005253309.1:c.1802A>G | XP_005253366.1:p.Tyr601Cys | |
| XM_005253310.3:c.1337A>G | XP_005253367.1:p.Tyr446Cys | |
| XM_011520554.1:c.2375A>G | XP_011518856.1:p.Tyr792Cys | |
| XM_011520555.1:c.2081A>G | XP_011518857.1:p.Tyr694Cys | |
| XM_011520556.1:c.2081A>G | XP_011518858.1:p.Tyr694Cys | |
| XM_011520557.1:c.1529A>G | XP_011518859.1:p.Tyr510Cys | |
| XM_011520558.1:c.1484A>G | XP_011518860.1:p.Tyr495Cys | |
| XM_011520559.1:c.1316A>G | XP_011518861.1:p.Tyr439Cys | |
| NM_001330373.1:c.1802A>G | NP_001317302.1:p.Tyr601Cys | |
| NM_001330374.1:c.1802A>G | NP_001317303.1:p.Tyr601Cys | |
| XM_005253304.4:c.2573A>G | XP_005253361.1:p.Tyr858Cys | |
| XM_005253308.5:c.1802A>G | XP_005253365.1:p.Tyr601Cys | |
| XM_005253310.4:c.1337A>G | XP_005253367.1:p.Tyr446Cys | |
| XM_011520558.2:c.1484A>G | XP_011518860.1:p.Tyr495Cys | |
| XM_011520559.3:c.1316A>G | XP_011518861.1:p.Tyr439Cys | |
| XM_017018803.1:c.2573A>G | XP_016874292.1:p.Tyr858Cys | |
| XM_017018805.1:c.1529A>G | XP_016874294.1:p.Tyr510Cys | |
| XM_024448837.1:c.1802A>G | XP_024304605.1:p.Tyr601Cys | |
| XM_024448838.1:c.1802A>G | XP_024304606.1:p.Tyr601Cys | |
| XM_024448839.1:c.1802A>G | XP_024304607.1:p.Tyr601Cys | |
| XM_024448840.1:c.1190A>G | XP_024304608.1:p.Tyr397Cys | |
| NM_001370297.1:c.1529A>G | NP_001357226.1:p.Tyr510Cys | |
| NM_001370298.1:c.2573A>G | NP_001357227.1:p.Tyr858Cys | |
| NM_001304484.2:c.1049A>G | NP_001291413.1:p.Tyr350Cys | |
| NM_001330373.2:c.1802A>G | NP_001317302.1:p.Tyr601Cys | |
| NM_001330374.2:c.1802A>G | NP_001317303.1:p.Tyr601Cys | |
| NM_001370298.3:c.2492A>G MANE Select | NP_001357227.2:p.Tyr831Cys | |
| NM_001384126.1:c.2492A>G | NP_001371055.1:p.Tyr831Cys | |
| NM_001384127.1:c.2081A>G | NP_001371056.1:p.Tyr694Cys | |
| NM_001384128.1:c.2081A>G | NP_001371057.1:p.Tyr694Cys | |
| NM_001384130.1:c.1802A>G | NP_001371059.1:p.Tyr601Cys | |
| NM_001385118.1:c.2081A>G | NP_001372047.1:p.Tyr694Cys |