Linked Data
ClinVar Variation Id:
302301
ClinVar RCV Id:
RCV000354364
dbSNP Id:
rs886047633
gnomAD v3:
11-110229812-A-G
gnomAD v4:
11-110229812-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.110229812A>G , CM000673.2:g.110229812A>G | GRCh38 |
| NC_000011.9:g.110100537A>G , CM000673.1:g.110100537A>G | GRCh37 |
| NC_000011.8:g.109605747A>G | NCBI36 |
| NG_023044.1:g.71901T>C | |
| NG_023044.2:g.71901T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000645312.1:c.391+2061T>C | ||
| ENST00000645495.2:c.*2057T>C MANE Select | ENSP00000496503.2:n.*2057T>C | |
| ENST00000645527.1:c.1587+3425T>C | ENSP00000496121.1:n.1587+3425T>C | |
| ENST00000646663.1:c.1748+2061T>C | ENSP00000494693.1:n.1748+2061T>C | |
| ENST00000647231.1:c.1748+2061T>C | ENSP00000496414.1:n.1748+2061T>C | |
| ENST00000343115.8:c.*2057T>C | ENSP00000342830.4:n.*2057T>C | |
| ENST00000405097.5:c.1748+2061T>C | ENSP00000384136.1:n.1748+2061T>C | |
| ENST00000527537.5:n.3038T>C | ||
| ENST00000528498.5:c.1748+2061T>C | ENSP00000432112.1:n.1748+2061T>C | |
| ENST00000528900.5:c.707+2061T>C | ENSP00000433580.1:n.707+2061T>C | |
| ENST00000530301.5:c.536+2061T>C | ENSP00000436277.1:n.536+2061T>C | |
| ENST00000530749.5:c.1748+2061T>C | ENSP00000437301.1:n.1748+2061T>C | |
| ENST00000532461.5:n.2924T>C | ||
| ENST00000544551.5:c.*2057T>C | ENSP00000445826.1:n.*2057T>C | |
| NM_001260492.1:c.1748+2061T>C | NP_001247421.1:n.1748+2061T>C | |
| NM_001260493.1:c.1748+2061T>C | NP_001247422.1:n.1748+2061T>C | |
| NM_001260494.1:c.*2057T>C | NP_001247423.1:n.*2057T>C | |
| NM_001260495.1:c.707+2061T>C | NP_001247424.1:n.707+2061T>C | |
| NM_001260496.1:c.536+2061T>C | NP_001247425.1:n.536+2061T>C | |
| NM_002906.3:c.*2057T>C | NP_002897.1:n.*2057T>C | |
| NM_001260492.2:c.1748+2061T>C | NP_001247421.1:n.1748+2061T>C | |
| NM_002906.4:c.*2057T>C MANE Select | NP_002897.1:n.*2057T>C | |
| NM_001260493.2:c.1748+2061T>C | NP_001247422.1:n.1748+2061T>C | |
| NM_001260494.2:c.*2057T>C | NP_001247423.1:n.*2057T>C | |
| NM_001260495.2:c.707+2061T>C | NP_001247424.1:n.707+2061T>C | |
| NM_001260496.2:c.536+2061T>C | NP_001247425.1:n.536+2061T>C |