Linked Data
ClinVar Variation Id:
623800
dbSNP Id:
rs1341534652
gnomAD v2:
12-32778673-C-T
gnomAD v3:
12-32625739-C-T
gnomAD v4:
12-32625739-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.32625739C>T , CM000674.2:g.32625739C>T | GRCh38 |
| NC_000012.11:g.32778673C>T , CM000674.1:g.32778673C>T | GRCh37 |
| NC_000012.10:g.32669940C>T | NCBI36 |
| NG_008626.2:g.231211C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000427716.7:c.1721C>T | ENSP00000394487.2:p.Ala574Val | |
| ENST00000531134.7:c.1976C>T | ENSP00000431323.1:p.Ala659Val | |
| ENST00000583694.2:c.1721C>T | ENSP00000462623.2:p.Ala574Val | |
| ENST00000682739.1:c.1442C>T | ENSP00000507616.1:p.Ala481Val | |
| ENST00000683182.1:c.533C>T | ENSP00000507831.1:p.Ala178Val | |
| ENST00000683515.1:n.1228C>T | ||
| ENST00000684033.1:n.519C>T | ||
| ENST00000525053.6:c.1721C>T | ENSP00000433666.2:p.Ala574Val | |
| ENST00000531134.6:c.1976C>T | ENSP00000431323.1:p.Ala659Val | |
| ENST00000534526.7:c.2132C>T MANE Select | ENSP00000449273.1:p.Ala711Val | |
| ENST00000395740.5:c.*1113C>T | ENSP00000379089.1:n.*1113C>T | |
| ENST00000427716.6:c.1721C>T | ENSP00000394487.2:p.Ala574Val | |
| ENST00000493087.5:c.*1132C>T | ENSP00000437109.1:n.*1132C>T | |
| ENST00000494977.1:c.1403C>T | ||
| ENST00000525053.5:c.2057C>T | ENSP00000433666.1:p.Ala686Val | |
| ENST00000531134.5:c.1976C>T | ENSP00000431323.1:p.Ala659Val | |
| ENST00000534526.6:c.2132C>T | ENSP00000449273.1:p.Ala711Val | |
| ENST00000546442.5:c.1442C>T | ENSP00000446695.1:p.Ala481Val | |
| ENST00000551984.5:c.*1090C>T | ENSP00000449614.1:n.*1090C>T | |
| NM_001304480.1:c.2057C>T | NP_001291409.1:p.Ala686Val | |
| NM_001304481.1:c.1976C>T | NP_001291410.1:p.Ala659Val | |
| NM_001304483.1:c.977C>T | NP_001291412.1:p.Ala326Val | |
| NM_001304484.1:c.689C>T | NP_001291413.1:p.Ala230Val | |
| NM_139241.3:c.1721C>T | NP_640334.2:p.Ala574Val | |
| XM_005253304.3:c.2213C>T | XP_005253361.1:p.Ala738Val | |
| XM_005253307.2:c.1442C>T | XP_005253364.1:p.Ala481Val | |
| XM_005253308.3:c.1442C>T | XP_005253365.1:p.Ala481Val | |
| XM_005253309.1:c.1442C>T | XP_005253366.1:p.Ala481Val | |
| XM_005253310.3:c.977C>T | XP_005253367.1:p.Ala326Val | |
| XM_011520554.1:c.2015C>T | XP_011518856.1:p.Ala672Val | |
| XM_011520555.1:c.1721C>T | XP_011518857.1:p.Ala574Val | |
| XM_011520556.1:c.1721C>T | XP_011518858.1:p.Ala574Val | |
| XM_011520557.1:c.1169C>T | XP_011518859.1:p.Ala390Val | |
| XM_011520558.1:c.1124C>T | XP_011518860.1:p.Ala375Val | |
| XM_011520559.1:c.956C>T | XP_011518861.1:p.Ala319Val | |
| NM_001330373.1:c.1442C>T | NP_001317302.1:p.Ala481Val | |
| NM_001330374.1:c.1442C>T | NP_001317303.1:p.Ala481Val | |
| XM_005253304.4:c.2213C>T | XP_005253361.1:p.Ala738Val | |
| XM_005253308.5:c.1442C>T | XP_005253365.1:p.Ala481Val | |
| XM_005253310.4:c.977C>T | XP_005253367.1:p.Ala326Val | |
| XM_011520558.2:c.1124C>T | XP_011518860.1:p.Ala375Val | |
| XM_011520559.3:c.956C>T | XP_011518861.1:p.Ala319Val | |
| XM_017018803.1:c.2213C>T | XP_016874292.1:p.Ala738Val | |
| XM_017018805.1:c.1169C>T | XP_016874294.1:p.Ala390Val | |
| XM_024448837.1:c.1442C>T | XP_024304605.1:p.Ala481Val | |
| XM_024448838.1:c.1442C>T | XP_024304606.1:p.Ala481Val | |
| XM_024448839.1:c.1442C>T | XP_024304607.1:p.Ala481Val | |
| XM_024448840.1:c.830C>T | XP_024304608.1:p.Ala277Val | |
| NM_001370297.1:c.1169C>T | NP_001357226.1:p.Ala390Val | |
| NM_001370298.1:c.2213C>T | NP_001357227.1:p.Ala738Val | |
| NM_001304483.2:c.977C>T | NP_001291412.1:p.Ala326Val | |
| NM_001304484.2:c.689C>T | NP_001291413.1:p.Ala230Val | |
| NM_001330373.2:c.1442C>T | NP_001317302.1:p.Ala481Val | |
| NM_001330374.2:c.1442C>T | NP_001317303.1:p.Ala481Val | |
| NM_001370298.3:c.2132C>T MANE Select | NP_001357227.2:p.Ala711Val | |
| NM_001384126.1:c.2132C>T | NP_001371055.1:p.Ala711Val | |
| NM_001384127.1:c.1721C>T | NP_001371056.1:p.Ala574Val | |
| NM_001384128.1:c.1721C>T | NP_001371057.1:p.Ala574Val | |
| NM_001384130.1:c.1442C>T | NP_001371059.1:p.Ala481Val | |
| NM_001385118.1:c.1721C>T | NP_001372047.1:p.Ala574Val |