Linked Data
ClinVar Variation Id:
1122901
dbSNP Id:
rs769736716
ExAC:
16:14042060 C / T
gnomAD v2:
16-14042060-C-T
gnomAD v3:
16-13948203-C-T
gnomAD v4:
16-13948203-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13948203C>T , CM000678.2:g.13948203C>T | GRCh38 |
| NC_000016.9:g.14042060C>T , CM000678.1:g.14042060C>T | GRCh37 |
| NC_000016.8:g.13949561C>T | NCBI36 |
| NG_011442.1:g.33047C>T , LRG_463:g.33047C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682617.1:c.2745C>T | ENSP00000507912.1:p.His915= | |
| ENST00000683962.1:c.*2301C>T | ENSP00000506854.1:n.*2301C>T | |
| ENST00000311895.8:c.2607C>T MANE Select | ENSP00000310520.7:p.His869= | |
| ENST00000311895.7:c.2607C>T | ENSP00000310520.7:p.His869= | |
| ENST00000389138.7:n.1884C>T | ||
| NM_005236.2:c.2607C>T , LRG_463t1:c.2607C>T | NP_005227.1:p.His869= | |
| XM_011522424.1:c.2745C>T | XP_011520726.1:p.His915= | |
| XM_011522425.1:c.2064C>T | XP_011520727.1:p.His688= | |
| XM_011522426.1:c.1818C>T | XP_011520728.1:p.His606= | |
| XM_011522427.1:c.1257C>T | XP_011520729.1:p.His419= | |
| XR_932805.1:n.2766C>T | ||
| XM_011522424.3:c.2745C>T | XP_011520726.1:p.His915= | |
| XM_017023043.2:c.1818C>T | XP_016878532.1:p.His606= | |
| NM_005236.3:c.2607C>T MANE Select | NP_005227.1:p.His869= |