Linked Data
dbSNP Id:
rs1017750575
gnomAD v2:
22-20779425-G-C
gnomAD v3:
22-20425135-G-C
gnomAD v4:
22-20425135-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20425135G>C , CM000684.2:g.20425135G>C | GRCh38 |
| NC_000022.10:g.20779425G>C , CM000684.1:g.20779425G>C | GRCh37 |
| NC_000022.9:g.19109425G>C | NCBI36 |
| NG_031868.2:g.17725C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622235.5:c.*240C>G MANE Select | ENSP00000477564.2:n.*240C>G | |
| ENST00000615031.4:c.*240C>G | ENSP00000479389.1:n.*240C>G | |
| ENST00000622235.4:c.*240C>G | ENSP00000477564.1:n.*240C>G | |
| ENST00000623402.1:c.*240C>G | ENSP00000485276.1:n.*240C>G | |
| NM_153334.6:c.*240C>G | NP_699165.3:n.*240C>G | |
| NM_182895.4:c.*240C>G | NP_878315.2:n.*240C>G | |
| NM_153334.7:c.*240C>G | NP_699165.3:n.*240C>G | |
| NM_182895.5:c.*240C>G MANE Select | NP_878315.2:n.*240C>G |