Linked Data
ClinVar Variation Id:
303794
ClinVar RCV Id:
RCV000307844
dbSNP Id:
rs11827649
gnomAD v2:
11-17515474-G-C
gnomAD v3:
11-17493927-G-C
gnomAD v4:
11-17493927-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17493927G>C , CM000673.2:g.17493927G>C | GRCh38 |
| NC_000011.9:g.17515474G>C , CM000673.1:g.17515474G>C | GRCh37 |
| NC_000011.8:g.17472050G>C | NCBI36 |
| NG_011883.1:g.55490C>G | |
| NG_011883.2:g.55490C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000005226.12:c.*405C>G MANE Select | ENSP00000005226.7:n.*405C>G | |
| ENST00000318024.9:c.*437C>G MANE Plus Clinical | ENSP00000317018.4:n.*437C>G | |
| ENST00000318024.8:c.*437C>G | ENSP00000317018.4:n.*437C>G | |
| ENST00000526313.5:c.*810C>G | ENSP00000432236.1:n.*810C>G | |
| ENST00000527020.5:c.*437C>G | ENSP00000436934.1:n.*437C>G | |
| ENST00000527720.5:c.*437C>G | ENSP00000432944.1:n.*437C>G | |
| ENST00000624811.1:n.1167C>G | ||
| NM_001297764.1:c.*437C>G | NP_001284693.1:n.*437C>G | |
| NM_005709.3:c.*437C>G | NP_005700.2:n.*437C>G | |
| NM_153676.3:c.*405C>G | NP_710142.1:n.*405C>G | |
| NR_123738.1:n.2131C>G | ||
| XM_011519831.1:c.*437C>G | XP_011518133.1:n.*437C>G | |
| XM_011519832.1:c.*437C>G | XP_011518134.1:n.*437C>G | |
| XM_011519832.3:c.*437C>G | XP_011518134.1:n.*437C>G | |
| XR_001747717.2:n.2255C>G | ||
| NM_153676.4:c.*405C>G MANE Select | NP_710142.1:n.*405C>G | |
| NM_001297764.2:c.*437C>G | NP_001284693.1:n.*437C>G | |
| NM_005709.4:c.*437C>G MANE Plus Clinical | NP_005700.2:n.*437C>G | |
| NR_123738.2:n.2131C>G |