Linked Data
ClinVar Variation Id:
17995
dbSNP Id:
rs121912708
ExAC:
5:125919689 G / A
gnomAD v2:
5-125919689-G-A
gnomAD v3:
5-126583997-G-A
gnomAD v4:
5-126583997-G-A
PubMed:
PMID:16491085
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.126583997G>A , CM000667.2:g.126583997G>A | GRCh38 |
| NC_000005.9:g.125919689G>A , CM000667.1:g.125919689G>A | GRCh37 |
| NC_000005.8:g.125947588G>A | NCBI36 |
| NG_008600.2:g.16394C>T | |
| NG_008600.3:g.16394C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409134.8:c.328C>T MANE Select | ENSP00000387123.3:p.Arg110Ter | |
| ENST00000412186.2:c.328C>T | ENSP00000414536.2:p.Arg110Ter | |
| ENST00000413020.6:c.328C>T | ENSP00000487936.1:p.Arg110Ter | |
| ENST00000458249.6:c.*237C>T | ENSP00000403929.1:n.*237C>T | |
| ENST00000479989.6:n.511C>T | ||
| ENST00000503281.6:c.107-6786C>T | ||
| ENST00000509270.2:c.262C>T | ENSP00000449318.2:p.Arg88Ter | |
| ENST00000509459.6:c.66-6786C>T | ||
| ENST00000511266.6:n.1050C>T | ||
| ENST00000635851.1:c.326C>T | ||
| ENST00000636062.1:n.223C>T | ||
| ENST00000636190.1:n.207C>T | ||
| ENST00000636225.1:c.*137C>T | ENSP00000490797.1:n.*137C>T | |
| ENST00000636286.1:n.46C>T | ||
| ENST00000636743.1:c.208C>T | ENSP00000489725.1:p.Arg70Ter | |
| ENST00000636808.1:c.*137C>T | ENSP00000490833.1:n.*137C>T | |
| ENST00000636872.1:c.488C>T | ENSP00000490919.1:n.488C>T | |
| ENST00000636879.1:c.328C>T | ENSP00000490811.1:p.Arg110Ter | |
| ENST00000636886.1:c.193-1023C>T | ENSP00000490371.1:n.193-1023C>T | |
| ENST00000637206.1:c.328C>T | ENSP00000489895.1:p.Arg110Ter | |
| ENST00000637272.1:c.328C>T | ENSP00000489686.1:p.Arg110Ter | |
| ENST00000637782.1:c.328C>T | ENSP00000490024.1:p.Arg110Ter | |
| ENST00000637964.1:c.274C>T | ENSP00000490291.1:p.Arg92Ter | |
| ENST00000638008.1:c.*270C>T | ENSP00000490400.1:n.*270C>T | |
| ENST00000409134.7:c.328C>T | ENSP00000387123.3:p.Arg110Ter | |
| ENST00000412186.1:c.*137C>T | ENSP00000414536.1:n.*137C>T | |
| ENST00000413020.5:c.328C>T | ENSP00000487936.1:p.Arg110Ter | |
| ENST00000447989.6:c.409C>T | ENSP00000414132.2:p.Arg137Ter | |
| ENST00000458249.5:c.488C>T | ENSP00000403929.1:n.488C>T | |
| ENST00000479989.5:n.511C>T | ||
| ENST00000503281.5:c.107-6786C>T | ||
| ENST00000509270.1:c.208C>T | ENSP00000449318.1:p.Arg70Ter | |
| ENST00000509459.5:c.66-6786C>T | ||
| ENST00000510111.6:c.307-1023C>T | ENSP00000447388.1:n.307-1023C>T | |
| ENST00000511266.5:n.283C>T | ||
| ENST00000553117.5:c.328C>T | ENSP00000448593.1:p.Arg110Ter | |
| NM_001182.4:c.328C>T | NP_001173.2:p.Arg110Ter | |
| NM_001201377.1:c.244C>T | NP_001188306.1:p.Arg82Ter | |
| NM_001202404.1:c.409C>T | NP_001189333.1:p.Arg137Ter | |
| XM_011543417.1:c.-78C>T | XP_011541719.1:n.-78C>T | |
| XM_011543417.2:c.-78C>T | XP_011541719.1:n.-78C>T | |
| NM_001182.5:c.328C>T MANE Select | NP_001173.2:p.Arg110Ter | |
| NM_001201377.2:c.244C>T | NP_001188306.1:p.Arg82Ter | |
| NM_001202404.2:c.328C>T | NP_001189333.2:p.Arg110Ter |