Linked Data
ClinVar Variation Id:
259682
dbSNP Id:
rs9929524
ExAC:
16:14042215 C / T
gnomAD v2:
16-14042215-C-T
gnomAD v3:
16-13948358-C-T
gnomAD v4:
16-13948358-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13948358C>T , CM000678.2:g.13948358C>T | GRCh38 |
| NC_000016.9:g.14042215C>T , CM000678.1:g.14042215C>T | GRCh37 |
| NC_000016.8:g.13949716C>T | NCBI36 |
| NG_011442.1:g.33202C>T , LRG_463:g.33202C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682617.1:c.*11C>T | ENSP00000507912.1:n.*11C>T | |
| ENST00000683962.1:c.*2456C>T | ENSP00000506854.1:n.*2456C>T | |
| ENST00000311895.8:c.*11C>T MANE Select | ENSP00000310520.7:n.*11C>T | |
| ENST00000311895.7:c.*11C>T | ENSP00000310520.7:n.*11C>T | |
| ENST00000389138.7:n.2039C>T | ||
| NM_005236.2:c.*11C>T , LRG_463t1:c.*11C>T | NP_005227.1:n.*11C>T | |
| XM_011522424.1:c.*11C>T | XP_011520726.1:n.*11C>T | |
| XM_011522425.1:c.*11C>T | XP_011520727.1:n.*11C>T | |
| XM_011522426.1:c.*11C>T | XP_011520728.1:n.*11C>T | |
| XM_011522427.1:c.*11C>T | XP_011520729.1:n.*11C>T | |
| XR_932805.1:n.2921C>T | ||
| XM_011522424.3:c.*11C>T | XP_011520726.1:n.*11C>T | |
| XM_017023043.2:c.*11C>T | XP_016878532.1:n.*11C>T | |
| NM_005236.3:c.*11C>T MANE Select | NP_005227.1:n.*11C>T |