Linked Data
dbSNP Id:
rs766189378
ExAC:
21:38858959 C / G
gnomAD v2:
21-38858959-C-G
gnomAD v4:
21-37486657-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.37486657C>G , CM000683.2:g.37486657C>G | GRCh38 |
| NC_000021.8:g.38858959C>G , CM000683.1:g.38858959C>G | GRCh37 |
| NC_000021.7:g.37780829C>G | NCBI36 |
| NG_009366.1:g.124101C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338785.8:c.664+43C>G | ENSP00000342690.3:n.664+43C>G | |
| ENST00000398960.7:c.664+43C>G | ENSP00000381932.2:n.664+43C>G | |
| ENST00000642309.1:c.550+43C>G | ENSP00000495596.1:n.550+43C>G | |
| ENST00000643355.1:n.396C>G | ||
| ENST00000643624.1:c.637+43C>G | ENSP00000493627.1:n.637+43C>G | |
| ENST00000643808.1:n.467+43C>G | ||
| ENST00000643854.1:c.550+43C>G | ENSP00000493653.1:n.550+43C>G | |
| ENST00000644367.1:n.18C>G | ||
| ENST00000644942.1:c.664+43C>G | ENSP00000494544.1:n.664+43C>G | |
| ENST00000645424.1:c.664+43C>G | ENSP00000494897.1:n.664+43C>G | |
| ENST00000645774.1:c.685+43C>G | ENSP00000494536.1:n.685+43C>G | |
| ENST00000646523.1:c.664+43C>G | ENSP00000495632.1:n.664+43C>G | |
| ENST00000646548.1:c.637+43C>G | ENSP00000495908.1:n.637+43C>G | |
| ENST00000647188.2:c.637+43C>G MANE Select | ENSP00000494572.1:n.637+43C>G | |
| ENST00000647425.1:c.637+43C>G | ENSP00000496748.1:n.637+43C>G | |
| ENST00000647504.1:c.550+43C>G | ENSP00000495571.1:n.550+43C>G | |
| ENST00000338785.7:c.664+43C>G | ENSP00000342690.3:n.664+43C>G | |
| ENST00000339659.8:c.637+43C>G | ENSP00000340373.3:n.637+43C>G | |
| ENST00000398956.2:c.664+43C>G | ENSP00000381929.2:n.664+43C>G | |
| ENST00000398960.6:c.664+43C>G | ENSP00000381932.2:n.664+43C>G | |
| NM_001396.3:c.664+43C>G | NP_001387.2:n.664+43C>G | |
| NM_101395.2:c.664+43C>G | NP_567824.1:n.664+43C>G | |
| NM_130436.2:c.637+43C>G | NP_569120.1:n.637+43C>G | |
| NM_130438.2:c.664+43C>G | NP_569122.1:n.664+43C>G | |
| XM_005260931.3:c.577+43C>G | XP_005260988.1:n.577+43C>G | |
| XM_006723976.2:c.664+43C>G | XP_006724039.1:n.664+43C>G | |
| XM_006723977.2:c.664+43C>G | XP_006724040.1:n.664+43C>G | |
| XM_006723978.2:c.664+43C>G | XP_006724041.1:n.664+43C>G | |
| XM_006723979.2:c.637+43C>G | XP_006724042.1:n.637+43C>G | |
| XM_011529482.1:c.685+43C>G | XP_011527784.1:n.685+43C>G | |
| XM_011529483.1:c.664+43C>G | XP_011527785.1:n.664+43C>G | |
| XM_011529484.1:c.658+43C>G | XP_011527786.1:n.658+43C>G | |
| XM_011529485.1:c.550+43C>G | XP_011527787.1:n.550+43C>G | |
| XR_937703.1:n.706+582G>C | ||
| XR_937704.1:n.617+2895G>C | ||
| XR_937705.1:n.966G>C | ||
| NM_001347721.1:c.637+43C>G | NP_001334650.1:n.637+43C>G | |
| NM_001347722.1:c.637+43C>G | NP_001334651.1:n.637+43C>G | |
| NM_001347723.1:c.550+43C>G | NP_001334652.1:n.550+43C>G | |
| NM_001396.4:c.664+43C>G | NP_001387.2:n.664+43C>G | |
| XM_006723976.3:c.664+43C>G | XP_006724039.1:n.664+43C>G | |
| XM_006723977.3:c.664+43C>G | XP_006724040.1:n.664+43C>G | |
| XM_006723978.3:c.664+43C>G | XP_006724041.1:n.664+43C>G | |
| XM_011529483.2:c.664+43C>G | XP_011527785.1:n.664+43C>G | |
| XM_017028284.1:c.637+43C>G | XP_016883773.1:n.637+43C>G | |
| XM_017028286.2:c.577+43C>G | XP_016883775.1:n.577+43C>G | |
| XM_024452057.1:c.550+43C>G | XP_024307825.1:n.550+43C>G | |
| XR_001755034.1:n.138+2895G>C | ||
| NM_001347721.2:c.637+43C>G MANE Select | NP_001334650.1:n.637+43C>G | |
| NM_001347722.2:c.637+43C>G | NP_001334651.1:n.637+43C>G | |
| NM_001347723.2:c.550+43C>G | NP_001334652.1:n.550+43C>G | |
| NM_001396.5:c.664+43C>G | NP_001387.2:n.664+43C>G |