Linked Data
ClinVar Variation Id:
535969
dbSNP Id:
rs780682938
ExAC:
16:2122926 T / C
gnomAD v2:
16-2122926-T-C
gnomAD v3:
16-2072925-T-C
gnomAD v4:
16-2072925-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2072925T>C , CM000678.2:g.2072925T>C | GRCh38 |
| NC_000016.9:g.2122926T>C , CM000678.1:g.2122926T>C | GRCh37 |
| NC_000016.8:g.2062927T>C | NCBI36 |
| NG_005895.1:g.28620T>C , LRG_487:g.28620T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*844T>C | ENSP00000455997.2:n.*844T>C | |
| ENST00000642206.2:c.2342T>C | ENSP00000495146.2:p.Val781Ala | |
| ENST00000642365.2:c.2297T>C | ENSP00000495459.2:p.Val766Ala | |
| ENST00000644417.2:c.*1734T>C | ENSP00000493912.2:n.*1734T>C | |
| ENST00000646464.2:c.*1942T>C | ENSP00000496610.2:n.*1942T>C | |
| ENST00000219476.9:c.2297T>C MANE Select | ENSP00000219476.3:p.Val766Ala | |
| ENST00000350773.9:c.2297T>C | ENSP00000344383.4:p.Val766Ala | |
| ENST00000401874.7:c.2297T>C | ENSP00000384468.2:p.Val766Ala | |
| ENST00000563346.2:n.475T>C | ||
| ENST00000568454.6:c.2330T>C | ENSP00000454487.1:p.Val777Ala | |
| ENST00000642365.1:c.954T>C | ||
| ENST00000642561.1:c.2297T>C | ENSP00000495099.1:p.Val766Ala | |
| ENST00000642797.1:c.2297T>C | ENSP00000493846.1:p.Val766Ala | |
| ENST00000642936.1:c.2297T>C | ENSP00000494514.1:p.Val766Ala | |
| ENST00000643088.1:c.2297T>C | ENSP00000494747.1:p.Val766Ala | |
| ENST00000643298.1:c.*1799T>C | ENSP00000494393.1:n.*1799T>C | |
| ENST00000643946.1:c.2297T>C | ENSP00000495927.1:p.Val766Ala | |
| ENST00000644043.1:c.2297T>C | ENSP00000496262.1:p.Val766Ala | |
| ENST00000644329.1:c.2297T>C | ENSP00000496611.1:p.Val766Ala | |
| ENST00000644335.1:c.2297T>C | ENSP00000496317.1:p.Val766Ala | |
| ENST00000644399.1:c.2290T>C | ||
| ENST00000644847.1:n.1289T>C | ||
| ENST00000645024.1:n.579T>C | ||
| ENST00000645552.1:n.577T>C | ||
| ENST00000646388.1:c.2297T>C | ENSP00000495921.1:p.Val766Ala | |
| ENST00000646464.1:c.390T>C | ENSP00000496610.1:n.390T>C | |
| ENST00000646634.1:n.1310T>C | ||
| ENST00000219476.7:c.2297T>C | ENSP00000219476.3:p.Val766Ala | |
| ENST00000350773.8:c.2297T>C | ENSP00000344383.4:p.Val766Ala | |
| ENST00000382538.10:c.2150T>C | ENSP00000371978.6:p.Val717Ala | |
| ENST00000401874.6:c.2297T>C | ENSP00000384468.2:p.Val766Ala | |
| ENST00000439117.6:c.*1596T>C | ENSP00000406980.2:n.*1596T>C | |
| ENST00000439673.6:c.2186T>C | ENSP00000399232.2:p.Val729Ala | |
| ENST00000463808.1:n.331T>C | ||
| ENST00000563346.1:n.366T>C | ||
| ENST00000568454.5:c.2330T>C | ENSP00000454487.1:p.Val777Ala | |
| NM_000548.3:c.2297T>C , LRG_487t1:c.2297T>C | NP_000539.2:p.Val766Ala | |
| NM_001077183.1:c.2297T>C | NP_001070651.1:p.Val766Ala | |
| NM_001114382.1:c.2297T>C | NP_001107854.1:p.Val766Ala | |
| XM_005255529.3:c.2297T>C | XP_005255586.2:p.Val766Ala | |
| XM_005255531.3:c.2297T>C | XP_005255588.2:p.Val766Ala | |
| XM_011522636.1:c.2297T>C | XP_011520938.1:p.Val766Ala | |
| XM_011522637.1:c.2297T>C | XP_011520939.1:p.Val766Ala | |
| XM_011522638.1:c.2186T>C | XP_011520940.1:p.Val729Ala | |
| XM_011522639.1:c.2297T>C | XP_011520941.1:p.Val766Ala | |
| XM_011522640.1:c.2297T>C | XP_011520942.1:p.Val766Ala | |
| XM_011522641.1:c.2186T>C | XP_011520943.1:p.Val729Ala | |
| NM_000548.4:c.2297T>C | NP_000539.2:p.Val766Ala | |
| NM_001077183.2:c.2297T>C | NP_001070651.1:p.Val766Ala | |
| NM_001114382.2:c.2297T>C | NP_001107854.1:p.Val766Ala | |
| NM_001318827.1:c.2186T>C | NP_001305756.1:p.Val729Ala | |
| NM_001318829.1:c.2150T>C | NP_001305758.1:p.Val717Ala | |
| NM_001318831.1:c.1697T>C | NP_001305760.1:p.Val566Ala | |
| NM_001318832.1:c.2330T>C | NP_001305761.1:p.Val777Ala | |
| NM_001363528.1:c.2297T>C | NP_001350457.1:p.Val766Ala | |
| NM_021055.2:c.2297T>C | NP_066399.2:p.Val766Ala | |
| XM_005255531.4:c.2297T>C | XP_005255588.2:p.Val766Ala | |
| XM_011522636.2:c.2297T>C | XP_011520938.1:p.Val766Ala | |
| XM_011522637.2:c.2297T>C | XP_011520939.1:p.Val766Ala | |
| XM_011522638.2:c.2459T>C | XP_011520940.2:p.Val820Ala | |
| XM_011522639.2:c.2297T>C | XP_011520941.1:p.Val766Ala | |
| XM_011522640.2:c.2297T>C | XP_011520942.1:p.Val766Ala | |
| XM_017023615.1:c.2297T>C | XP_016879104.1:p.Val766Ala | |
| XM_017023616.1:c.2297T>C | XP_016879105.1:p.Val766Ala | |
| XM_017023617.1:c.2459T>C | XP_016879106.1:p.Val820Ala | |
| XM_017023618.1:c.953T>C | XP_016879107.1:p.Val318Ala | |
| XM_024450413.1:c.2297T>C | XP_024306181.1:p.Val766Ala | |
| NM_000548.5:c.2297T>C MANE Select | NP_000539.2:p.Val766Ala | |
| NM_001370404.1:c.2297T>C | NP_001357333.1:p.Val766Ala | |
| NM_001370405.1:c.2297T>C | NP_001357334.1:p.Val766Ala | |
| NM_001077183.3:c.2297T>C | NP_001070651.1:p.Val766Ala | |
| NM_001114382.3:c.2297T>C | NP_001107854.1:p.Val766Ala | |
| NM_001318827.2:c.2186T>C | NP_001305756.1:p.Val729Ala | |
| NM_001318829.2:c.2150T>C | NP_001305758.1:p.Val717Ala | |
| NM_001318831.2:c.1697T>C | NP_001305760.1:p.Val566Ala | |
| NM_001318832.2:c.2330T>C | NP_001305761.1:p.Val777Ala | |
| NM_001363528.2:c.2297T>C | NP_001350457.1:p.Val766Ala | |
| NM_021055.3:c.2297T>C | NP_066399.2:p.Val766Ala |