Linked Data
ClinVar Variation Id:
162153
dbSNP Id:
rs724159949
gnomAD v2:
21-38858865-C-T
gnomAD v4:
21-37486563-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.37486563C>T , CM000683.2:g.37486563C>T | GRCh38 |
| NC_000021.8:g.38858865C>T , CM000683.1:g.38858865C>T | GRCh37 |
| NC_000021.7:g.37780735C>T | NCBI36 |
| NG_009366.1:g.124007C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338785.8:c.613C>T | ENSP00000342690.3:p.Arg205Ter | |
| ENST00000398960.7:c.613C>T | ENSP00000381932.2:p.Arg205Ter | |
| ENST00000642309.1:c.499C>T | ENSP00000495596.1:p.Arg167Ter | |
| ENST00000643355.1:n.302C>T | ||
| ENST00000643624.1:c.586C>T | ENSP00000493627.1:p.Arg196Ter | |
| ENST00000643808.1:n.416C>T | ||
| ENST00000643854.1:c.499C>T | ENSP00000493653.1:p.Arg167Ter | |
| ENST00000644942.1:c.613C>T | ENSP00000494544.1:p.Arg205Ter | |
| ENST00000645424.1:c.613C>T | ENSP00000494897.1:p.Arg205Ter | |
| ENST00000645774.1:c.634C>T | ENSP00000494536.1:p.Arg212Ter | |
| ENST00000646523.1:c.613C>T | ENSP00000495632.1:p.Arg205Ter | |
| ENST00000646548.1:c.586C>T | ENSP00000495908.1:p.Arg196Ter | |
| ENST00000647188.2:c.586C>T MANE Select | ENSP00000494572.1:p.Arg196Ter | |
| ENST00000647425.1:c.586C>T | ENSP00000496748.1:p.Arg196Ter | |
| ENST00000647504.1:c.499C>T | ENSP00000495571.1:p.Arg167Ter | |
| ENST00000338785.7:c.613C>T | ENSP00000342690.3:p.Arg205Ter | |
| ENST00000339659.8:c.586C>T | ENSP00000340373.3:p.Arg196Ter | |
| ENST00000398956.2:c.613C>T | ENSP00000381929.2:p.Arg205Ter | |
| ENST00000398960.6:c.613C>T | ENSP00000381932.2:p.Arg205Ter | |
| NM_001396.3:c.613C>T | NP_001387.2:p.Arg205Ter | |
| NM_101395.2:c.613C>T | NP_567824.1:p.Arg205Ter | |
| NM_130436.2:c.586C>T | NP_569120.1:p.Arg196Ter | |
| NM_130438.2:c.613C>T | NP_569122.1:p.Arg205Ter | |
| XM_005260931.3:c.526C>T | XP_005260988.1:p.Arg176Ter | |
| XM_006723976.2:c.613C>T | XP_006724039.1:p.Arg205Ter | |
| XM_006723977.2:c.613C>T | XP_006724040.1:p.Arg205Ter | |
| XM_006723978.2:c.613C>T | XP_006724041.1:p.Arg205Ter | |
| XM_006723979.2:c.586C>T | XP_006724042.1:p.Arg196Ter | |
| XM_011529482.1:c.634C>T | XP_011527784.1:p.Arg212Ter | |
| XM_011529483.1:c.613C>T | XP_011527785.1:p.Arg205Ter | |
| XM_011529484.1:c.607C>T | XP_011527786.1:p.Arg203Ter | |
| XM_011529485.1:c.499C>T | XP_011527787.1:p.Arg167Ter | |
| XR_937703.1:n.706+676G>A | ||
| XR_937704.1:n.617+2989G>A | ||
| NM_001347721.1:c.586C>T | NP_001334650.1:p.Arg196Ter | |
| NM_001347722.1:c.586C>T | NP_001334651.1:p.Arg196Ter | |
| NM_001347723.1:c.499C>T | NP_001334652.1:p.Arg167Ter | |
| NM_001396.4:c.613C>T | NP_001387.2:p.Arg205Ter | |
| XM_006723976.3:c.613C>T | XP_006724039.1:p.Arg205Ter | |
| XM_006723977.3:c.613C>T | XP_006724040.1:p.Arg205Ter | |
| XM_006723978.3:c.613C>T | XP_006724041.1:p.Arg205Ter | |
| XM_011529483.2:c.613C>T | XP_011527785.1:p.Arg205Ter | |
| XM_017028284.1:c.586C>T | XP_016883773.1:p.Arg196Ter | |
| XM_017028286.2:c.526C>T | XP_016883775.1:p.Arg176Ter | |
| XM_024452057.1:c.499C>T | XP_024307825.1:p.Arg167Ter | |
| XR_001755034.1:n.138+2989G>A | ||
| NM_001347721.2:c.586C>T MANE Select | NP_001334650.1:p.Arg196Ter | |
| NM_001347722.2:c.586C>T | NP_001334651.1:p.Arg196Ter | |
| NM_001347723.2:c.499C>T | NP_001334652.1:p.Arg167Ter | |
| NM_001396.5:c.613C>T | NP_001387.2:p.Arg205Ter |