Linked Data
ClinVar Variation Id:
245608
dbSNP Id:
rs770501034
ExAC:
8:75276294 C / T
gnomAD v2:
8-75276294-C-T
gnomAD v3:
8-74364059-C-T
gnomAD v4:
8-74364059-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.74364059C>T , CM000670.2:g.74364059C>T | GRCh38 |
| NC_000008.10:g.75276294C>T , CM000670.1:g.75276294C>T | GRCh37 |
| NC_000008.9:g.75438849C>T | NCBI36 |
| NG_008787.2:g.47930C>T | |
| NG_008787.3:g.47930C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220822.12:c.769C>T MANE Select | ENSP00000220822.7:p.Arg257Ter | |
| ENST00000434412.3:c.637C>T | ENSP00000417006.3:p.Arg213Ter | |
| ENST00000520797.6:n.880C>T | ||
| ENST00000521096.6:n.625C>T | ||
| ENST00000522568.2:c.*441C>T | ENSP00000430136.1:n.*441C>T | |
| ENST00000523640.2:c.165+12738C>T | ENSP00000502017.1:n.165+12738C>T | |
| ENST00000524195.2:c.280+1006C>T | ENSP00000502308.1:n.280+1006C>T | |
| ENST00000674612.1:c.442C>T | ENSP00000501864.1:p.Arg148Ter | |
| ENST00000674710.1:c.694+1006C>T | ENSP00000502762.1:n.694+1006C>T | |
| ENST00000674754.1:c.*2332C>T | ENSP00000502063.1:n.*2332C>T | |
| ENST00000674756.1:c.*366+1006C>T | ENSP00000501860.1:n.*366+1006C>T | |
| ENST00000674806.1:c.442C>T | ENSP00000502637.1:p.Arg148Ter | |
| ENST00000674865.1:c.565C>T | ENSP00000502437.1:p.Arg189Ter | |
| ENST00000674926.1:c.*1401C>T | ENSP00000501799.1:n.*1401C>T | |
| ENST00000674934.1:c.*457C>T | ENSP00000502187.1:n.*457C>T | |
| ENST00000674944.1:c.*1372C>T | ENSP00000501858.1:n.*1372C>T | |
| ENST00000674946.1:c.694+1006C>T | ENSP00000501569.1:n.694+1006C>T | |
| ENST00000674973.1:c.463C>T | ENSP00000502447.1:p.Arg155Ter | |
| ENST00000675007.1:c.*507C>T | ENSP00000502119.1:n.*507C>T | |
| ENST00000675060.1:c.*434C>T | ENSP00000501616.1:n.*434C>T | |
| ENST00000675165.1:c.766C>T | ENSP00000502612.1:p.Arg256Ter | |
| ENST00000675220.1:c.442C>T | ENSP00000502588.1:p.Arg148Ter | |
| ENST00000675265.1:c.*519C>T | ENSP00000501848.1:n.*519C>T | |
| ENST00000675336.1:c.*255C>T | ENSP00000502120.1:n.*255C>T | |
| ENST00000675376.1:c.442C>T | ENSP00000502838.1:p.Arg148Ter | |
| ENST00000675463.1:c.847C>T | ENSP00000502327.1:p.Arg283Ter | |
| ENST00000675472.1:c.*255C>T | ENSP00000501946.1:n.*255C>T | |
| ENST00000675474.1:n.354C>T | ||
| ENST00000675560.1:c.*366+1006C>T | ENSP00000502118.1:n.*366+1006C>T | |
| ENST00000675625.1:c.*441C>T | ENSP00000501626.1:n.*441C>T | |
| ENST00000675633.1:c.*176C>T | ENSP00000501785.1:n.*176C>T | |
| ENST00000675661.1:c.*529C>T | ENSP00000501958.1:n.*529C>T | |
| ENST00000675706.1:n.2727C>T | ||
| ENST00000675821.1:c.442C>T | ENSP00000502198.1:p.Arg148Ter | |
| ENST00000675832.1:c.*441C>T | ENSP00000502041.1:n.*441C>T | |
| ENST00000675928.1:c.595C>T | ENSP00000501568.1:p.Arg199Ter | |
| ENST00000675944.1:c.565C>T | ENSP00000502673.1:p.Arg189Ter | |
| ENST00000675999.1:c.694+1006C>T | ENSP00000502572.1:n.694+1006C>T | |
| ENST00000676049.1:c.*671C>T | ENSP00000501912.1:n.*671C>T | |
| ENST00000676112.1:c.835C>T | ENSP00000502295.1:p.Arg279Ter | |
| ENST00000676143.1:c.442C>T | ENSP00000502828.1:p.Arg148Ter | |
| ENST00000676207.1:c.694+1006C>T | ENSP00000502638.1:n.694+1006C>T | |
| ENST00000676377.1:c.442C>T | ENSP00000502756.1:p.Arg148Ter | |
| ENST00000676415.1:c.*75C>T | ENSP00000502665.1:n.*75C>T | |
| ENST00000676443.1:c.721C>T | ENSP00000501769.1:p.Arg241Ter | |
| ENST00000220822.11:c.769C>T | ENSP00000220822.7:p.Arg257Ter | |
| ENST00000434412.2:c.565C>T | ENSP00000417006.2:p.Arg189Ter | |
| ENST00000520797.5:n.534C>T | ||
| ENST00000521096.5:n.575C>T | ||
| ENST00000522568.1:c.*441C>T | ENSP00000430136.1:n.*441C>T | |
| ENST00000524195.1:n.103+1006C>T | ||
| NM_001040875.2:c.565C>T | NP_001035808.1:p.Arg189Ter | |
| NM_018972.2:c.769C>T | NP_061845.2:p.Arg257Ter | |
| NR_046346.1:n.703C>T | ||
| XM_011517551.1:c.1063C>T | XP_011515853.1:p.Arg355Ter | |
| XM_011517552.1:c.442C>T | XP_011515854.1:p.Arg148Ter | |
| NM_001040875.3:c.565C>T | NP_001035808.1:p.Arg189Ter | |
| NM_001362929.1:c.442C>T | NP_001349858.1:p.Arg148Ter | |
| NM_001362930.1:c.595C>T | NP_001349859.1:p.Arg199Ter | |
| NM_001362931.1:c.694+1006C>T | NP_001349860.1:n.694+1006C>T | |
| NM_001362932.1:c.442C>T | NP_001349861.1:p.Arg148Ter | |
| NM_018972.3:c.769C>T | NP_061845.2:p.Arg257Ter | |
| NM_001362931.2:c.694+1006C>T | NP_001349860.1:n.694+1006C>T | |
| NM_018972.4:c.769C>T MANE Select | NP_061845.2:p.Arg257Ter | |
| NM_001040875.4:c.565C>T | NP_001035808.1:p.Arg189Ter | |
| NM_001362929.2:c.442C>T | NP_001349858.1:p.Arg148Ter | |
| NM_001362930.2:c.595C>T | NP_001349859.1:p.Arg199Ter | |
| NM_001362932.2:c.442C>T | NP_001349861.1:p.Arg148Ter |