Linked Data
ClinVar Variation Id:
380372
dbSNP Id:
rs9282652
ExAC:
16:68867409 C / T
gnomAD v2:
16-68867409-C-T
gnomAD v3:
16-68833506-C-T
gnomAD v4:
16-68833506-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68833506C>T , CM000678.2:g.68833506C>T | GRCh38 |
| NC_000016.9:g.68867409C>T , CM000678.1:g.68867409C>T | GRCh37 |
| NC_000016.8:g.67424910C>T | NCBI36 |
| NG_008021.1:g.101215C>T , LRG_301:g.101215C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.*7C>T MANE Select | ENSP00000261769.4:n.*7C>T | |
| ENST00000261769.9:c.*7C>T | ENSP00000261769.4:n.*7C>T | |
| ENST00000422392.6:c.*7C>T | ENSP00000414946.2:n.*7C>T | |
| ENST00000562118.1:n.874C>T | ||
| ENST00000562836.5:n.2727C>T | ||
| ENST00000566510.5:c.*1322C>T | ENSP00000458139.1:n.*1322C>T | |
| ENST00000566612.5:c.*896C>T | ENSP00000454782.1:n.*896C>T | |
| ENST00000611625.4:c.*7C>T | ENSP00000481063.1:n.*7C>T | |
| ENST00000612417.4:c.1854-685C>T | ENSP00000478360.1:n.1854-685C>T | |
| ENST00000621016.4:c.1866-697C>T | ENSP00000480664.1:n.1866-697C>T | |
| NM_004360.3:c.*7C>T , LRG_301t1:c.*7C>T | NP_004351.1:n.*7C>T | |
| XM_011523488.1:c.*7C>T | XP_011521790.1:n.*7C>T | |
| XM_011523489.1:c.*7C>T | XP_011521791.1:n.*7C>T | |
| NM_001317184.1:c.*7C>T | NP_001304113.1:n.*7C>T | |
| NM_001317185.1:c.*7C>T | NP_001304114.1:n.*7C>T | |
| NM_001317186.1:c.*7C>T | NP_001304115.1:n.*7C>T | |
| NM_004360.4:c.*7C>T | NP_004351.1:n.*7C>T | |
| NM_004360.5:c.*7C>T MANE Select | NP_004351.1:n.*7C>T | |
| NM_001317184.2:c.*7C>T | NP_001304113.1:n.*7C>T | |
| NM_001317185.2:c.*7C>T | NP_001304114.1:n.*7C>T | |
| NM_001317186.2:c.*7C>T | NP_001304115.1:n.*7C>T |