Linked Data
ClinVar Variation Id:
310311
dbSNP Id:
rs886049798
gnomAD v2:
12-66859048-T-C
gnomAD v3:
12-66465268-T-C
gnomAD v4:
12-66465268-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.66465268T>C , CM000674.2:g.66465268T>C | GRCh38 |
| NC_000012.11:g.66859048T>C , CM000674.1:g.66859048T>C | GRCh37 |
| NC_000012.10:g.65145315T>C | NCBI36 |
| NG_021400.1:g.218878A>G | |
| NG_021400.2:g.608998A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696989.1:c.1097+7A>G | ENSP00000513025.1:n.1097+7A>G | |
| ENST00000359742.9:c.872+7A>G MANE Select | ENSP00000352780.4:n.872+7A>G | |
| ENST00000359742.8:c.872+7A>G | ENSP00000352780.4:n.872+7A>G | |
| ENST00000398016.7:c.872+7A>G | ENSP00000381098.3:n.872+7A>G | |
| ENST00000535002.1:c.148+7A>G | ||
| ENST00000536215.5:c.704+7A>G | ENSP00000446011.1:n.704+7A>G | |
| ENST00000538164.5:c.316+7A>G | ||
| ENST00000538211.5:c.872+7A>G | ENSP00000446047.1:n.872+7A>G | |
| ENST00000540433.5:c.704+7A>G | ENSP00000446024.1:n.704+7A>G | |
| ENST00000540854.5:c.337+50351A>G | ENSP00000443006.1:n.337+50351A>G | |
| ENST00000543172.5:c.333+7A>G | ||
| NM_001178074.1:c.872+7A>G | NP_001171545.1:n.872+7A>G | |
| NM_021150.3:c.872+7A>G | NP_066973.2:n.872+7A>G | |
| XM_005268754.3:c.875+7A>G | XP_005268811.1:n.875+7A>G | |
| XM_005268757.3:c.794+7A>G | XP_005268814.1:n.794+7A>G | |
| XM_011538089.1:c.1097+7A>G | XP_011536391.1:n.1097+7A>G | |
| XM_011538090.1:c.1097+7A>G | XP_011536392.1:n.1097+7A>G | |
| XM_011538091.1:c.1097+7A>G | XP_011536393.1:n.1097+7A>G | |
| XM_011538092.1:c.1097+7A>G | XP_011536394.1:n.1097+7A>G | |
| XM_011538093.1:c.872+7A>G | XP_011536395.1:n.872+7A>G | |
| XM_011538094.1:c.704+7A>G | XP_011536396.1:n.704+7A>G | |
| NM_001366722.1:c.872+7A>G MANE Select | NP_001353651.1:n.872+7A>G | |
| NM_001366723.1:c.950+7A>G | NP_001353652.1:n.950+7A>G | |
| NM_001366724.1:c.950+7A>G | NP_001353653.1:n.950+7A>G | |
| XM_005268754.4:c.875+7A>G | XP_005268811.1:n.875+7A>G | |
| XM_005268757.4:c.794+7A>G | XP_005268814.1:n.794+7A>G | |
| XM_017019098.1:c.1097+7A>G | XP_016874587.1:n.1097+7A>G | |
| XM_017019099.1:c.950+7A>G | XP_016874588.1:n.950+7A>G | |
| XM_017019100.1:c.1097+7A>G | XP_016874589.1:n.1097+7A>G | |
| NM_001178074.2:c.872+7A>G | NP_001171545.1:n.872+7A>G | |
| NM_021150.4:c.872+7A>G | NP_066973.2:n.872+7A>G | |
| NM_001379345.1:c.950+7A>G | NP_001366274.1:n.950+7A>G | |
| NM_001379346.1:c.872+7A>G | NP_001366275.1:n.872+7A>G | |
| NM_001379347.1:c.950+7A>G | NP_001366276.1:n.950+7A>G | |
| NM_001379348.1:c.950+7A>G | NP_001366277.1:n.950+7A>G | |
| NM_001379349.1:c.875+7A>G | NP_001366278.1:n.875+7A>G | |
| NM_001379351.1:c.875+7A>G | NP_001366280.1:n.875+7A>G |