Linked Data
ClinVar Variation Id:
873391
dbSNP Id:
rs151257298
ExAC:
16:2156588 G / A
gnomAD v2:
16-2156588-G-A
gnomAD v4:
16-2106587-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2106587G>A , CM000678.2:g.2106587G>A | GRCh38 |
| NC_000016.9:g.2156588G>A , CM000678.1:g.2156588G>A | GRCh37 |
| NC_000016.8:g.2096589G>A | NCBI36 |
| NG_008617.1:g.34312C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262304.9:c.7300C>T MANE Select | ENSP00000262304.4:p.Arg2434Trp | |
| ENST00000262304.8:c.7300C>T | ENSP00000262304.4:p.Arg2434Trp | |
| ENST00000415938.7:n.545C>T | ||
| ENST00000423118.5:c.7300C>T | ENSP00000399501.1:p.Arg2434Trp | |
| ENST00000483558.5:n.359C>T | ||
| ENST00000483731.5:n.1025C>T | ||
| ENST00000486339.6:n.1046C>T | ||
| ENST00000487932.5:c.1987C>T | ENSP00000457132.1:p.Arg663Trp | |
| ENST00000496574.6:n.1303C>T | ||
| ENST00000565639.6:n.1008C>T | ||
| ENST00000568591.5:c.2461C>T | ENSP00000457162.1:n.2461C>T | |
| ENST00000569983.5:n.656C>T | ||
| NM_000296.3:c.7300C>T | NP_000287.3:p.Arg2434Trp | |
| NM_001009944.2:c.7300C>T | NP_001009944.2:p.Arg2434Trp | |
| XM_005255370.2:c.4255C>T | XP_005255427.1:p.Arg1419Trp | |
| XM_011522525.1:c.7378C>T | XP_011520827.1:p.Arg2460Trp | |
| XM_011522526.1:c.7378C>T | XP_011520828.1:p.Arg2460Trp | |
| XM_011522527.1:c.7378C>T | XP_011520829.1:p.Arg2460Trp | |
| XM_011522528.1:c.7354C>T | XP_011520830.1:p.Arg2452Trp | |
| XM_011522529.1:c.7354C>T | XP_011520831.1:p.Arg2452Trp | |
| XM_011522530.1:c.7324C>T | XP_011520832.1:p.Arg2442Trp | |
| XM_011522531.1:c.7306C>T | XP_011520833.1:p.Arg2436Trp | |
| XM_011522532.1:c.7252C>T | XP_011520834.1:p.Arg2418Trp | |
| XM_011522533.1:c.7171C>T | XP_011520835.1:p.Arg2391Trp | |
| XM_011522534.1:c.7114C>T | XP_011520836.1:p.Arg2372Trp | |
| XM_011522535.1:c.5200C>T | XP_011520837.1:p.Arg1734Trp | |
| XM_011522536.1:c.7378C>T | XP_011520838.1:p.Arg2460Trp | |
| XM_011522537.1:c.4378C>T | XP_011520839.1:p.Arg1460Trp | |
| XR_932867.1:n.7393C>T | ||
| XR_932868.1:n.7393C>T | ||
| XR_932869.1:n.7393C>T | ||
| XR_932870.1:n.7393C>T | ||
| XM_005255370.3:c.4255C>T | XP_005255427.1:p.Arg1419Trp | |
| XM_011522528.3:c.7354C>T | XP_011520830.1:p.Arg2452Trp | |
| XM_011522529.2:c.7354C>T | XP_011520831.1:p.Arg2452Trp | |
| XM_011522537.2:c.4378C>T | XP_011520839.1:p.Arg1460Trp | |
| XM_024450298.1:c.7420C>T | XP_024306066.1:p.Arg2474Trp | |
| XM_024450299.1:c.7348C>T | XP_024306067.1:p.Arg2450Trp | |
| XM_024450300.1:c.7210C>T | XP_024306068.1:p.Arg2404Trp | |
| XM_024450301.1:c.5296C>T | XP_024306069.1:p.Arg1766Trp | |
| NM_000296.4:c.7300C>T | NP_000287.4:p.Arg2434Trp | |
| NM_001009944.3:c.7300C>T MANE Select | NP_001009944.3:p.Arg2434Trp |