Linked Data
ClinVar Variation Id:
1546812
ClinVar RCV Id:
RCV002175034
dbSNP Id:
rs1310426800
gnomAD v2:
21-38862466-T-C
gnomAD v4:
21-37490164-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.37490164T>C , CM000683.2:g.37490164T>C | GRCh38 |
| NC_000021.8:g.38862466T>C , CM000683.1:g.38862466T>C | GRCh37 |
| NC_000021.7:g.37784336T>C | NCBI36 |
| NG_009366.1:g.127608T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338785.8:c.665-11T>C | ENSP00000342690.3:n.665-11T>C | |
| ENST00000398960.7:c.665-11T>C | ENSP00000381932.2:n.665-11T>C | |
| ENST00000642309.1:c.551-11T>C | ENSP00000495596.1:n.551-11T>C | |
| ENST00000643624.1:c.638-11T>C | ENSP00000493627.1:n.638-11T>C | |
| ENST00000643808.1:n.468-11T>C | ||
| ENST00000643854.1:c.551-11T>C | ENSP00000493653.1:n.551-11T>C | |
| ENST00000644367.1:n.29-11T>C | ||
| ENST00000644942.1:c.665-11T>C | ENSP00000494544.1:n.665-11T>C | |
| ENST00000645424.1:c.665-11T>C | ENSP00000494897.1:n.665-11T>C | |
| ENST00000645774.1:c.686-11T>C | ENSP00000494536.1:n.686-11T>C | |
| ENST00000646224.1:n.80-11T>C | ||
| ENST00000646523.1:c.665-11T>C | ENSP00000495632.1:n.665-11T>C | |
| ENST00000646548.1:c.638-11T>C | ENSP00000495908.1:n.638-11T>C | |
| ENST00000647188.2:c.638-11T>C MANE Select | ENSP00000494572.1:n.638-11T>C | |
| ENST00000647425.1:c.638-11T>C | ENSP00000496748.1:n.638-11T>C | |
| ENST00000647504.1:c.551-11T>C | ENSP00000495571.1:n.551-11T>C | |
| ENST00000338785.7:c.665-11T>C | ENSP00000342690.3:n.665-11T>C | |
| ENST00000339659.8:c.638-11T>C | ENSP00000340373.3:n.638-11T>C | |
| ENST00000398956.2:c.665-11T>C | ENSP00000381929.2:n.665-11T>C | |
| ENST00000398960.6:c.665-11T>C | ENSP00000381932.2:n.665-11T>C | |
| NM_001396.3:c.665-11T>C | NP_001387.2:n.665-11T>C | |
| NM_101395.2:c.665-11T>C | NP_567824.1:n.665-11T>C | |
| NM_130436.2:c.638-11T>C | NP_569120.1:n.638-11T>C | |
| NM_130438.2:c.665-11T>C | NP_569122.1:n.665-11T>C | |
| XM_005260931.3:c.578-11T>C | XP_005260988.1:n.578-11T>C | |
| XM_005260933.3:c.-20-11T>C | XP_005260990.1:n.-20-11T>C | |
| XM_006723976.2:c.665-11T>C | XP_006724039.1:n.665-11T>C | |
| XM_006723977.2:c.665-11T>C | XP_006724040.1:n.665-11T>C | |
| XM_006723978.2:c.665-11T>C | XP_006724041.1:n.665-11T>C | |
| XM_006723979.2:c.638-11T>C | XP_006724042.1:n.638-11T>C | |
| XM_011529482.1:c.686-11T>C | XP_011527784.1:n.686-11T>C | |
| XM_011529483.1:c.665-11T>C | XP_011527785.1:n.665-11T>C | |
| XM_011529484.1:c.659-11T>C | XP_011527786.1:n.659-11T>C | |
| XM_011529485.1:c.551-11T>C | XP_011527787.1:n.551-11T>C | |
| XR_937703.1:n.5A>G | ||
| XR_937704.1:n.5A>G | ||
| XR_937705.1:n.5A>G | ||
| NM_001347721.1:c.638-11T>C | NP_001334650.1:n.638-11T>C | |
| NM_001347722.1:c.638-11T>C | NP_001334651.1:n.638-11T>C | |
| NM_001347723.1:c.551-11T>C | NP_001334652.1:n.551-11T>C | |
| NM_001396.4:c.665-11T>C | NP_001387.2:n.665-11T>C | |
| XM_005260933.5:c.-20-11T>C | XP_005260990.1:n.-20-11T>C | |
| XM_006723976.3:c.665-11T>C | XP_006724039.1:n.665-11T>C | |
| XM_006723977.3:c.665-11T>C | XP_006724040.1:n.665-11T>C | |
| XM_006723978.3:c.665-11T>C | XP_006724041.1:n.665-11T>C | |
| XM_011529483.2:c.665-11T>C | XP_011527785.1:n.665-11T>C | |
| XM_017028284.1:c.638-11T>C | XP_016883773.1:n.638-11T>C | |
| XM_017028286.2:c.578-11T>C | XP_016883775.1:n.578-11T>C | |
| XM_024452057.1:c.551-11T>C | XP_024307825.1:n.551-11T>C | |
| XR_002958655.1:n.5A>G | ||
| NM_001347721.2:c.638-11T>C MANE Select | NP_001334650.1:n.638-11T>C | |
| NM_001347722.2:c.638-11T>C | NP_001334651.1:n.638-11T>C | |
| NM_001347723.2:c.551-11T>C | NP_001334652.1:n.551-11T>C | |
| NM_001396.5:c.665-11T>C | NP_001387.2:n.665-11T>C |