Linked Data
ClinVar Variation Id:
541253
dbSNP Id:
rs373237850
ExAC:
16:14038658 A / G
gnomAD v2:
16-14038658-A-G
gnomAD v3:
16-13944801-A-G
gnomAD v4:
16-13944801-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13944801A>G , CM000678.2:g.13944801A>G | GRCh38 |
| NC_000016.9:g.14038658A>G , CM000678.1:g.14038658A>G | GRCh37 |
| NC_000016.8:g.13946159A>G | NCBI36 |
| NG_011442.1:g.29645A>G , LRG_463:g.29645A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682617.1:c.2121A>G | ENSP00000507912.1:p.Ala707= | |
| ENST00000683962.1:c.*1677A>G | ENSP00000506854.1:n.*1677A>G | |
| ENST00000311895.8:c.1983A>G MANE Select | ENSP00000310520.7:p.Ala661= | |
| ENST00000311895.7:c.1983A>G | ENSP00000310520.7:p.Ala661= | |
| ENST00000389138.7:n.1260A>G | ||
| ENST00000462862.1:c.296A>G | ENSP00000461322.1:n.296A>G | |
| NM_005236.2:c.1983A>G , LRG_463t1:c.1983A>G | NP_005227.1:p.Ala661= | |
| XM_011522424.1:c.2121A>G | XP_011520726.1:p.Ala707= | |
| XM_011522425.1:c.1440A>G | XP_011520727.1:p.Ala480= | |
| XM_011522426.1:c.1194A>G | XP_011520728.1:p.Ala398= | |
| XM_011522427.1:c.633A>G | XP_011520729.1:p.Ala211= | |
| XR_932805.1:n.2142A>G | ||
| XM_011522424.3:c.2121A>G | XP_011520726.1:p.Ala707= | |
| XM_017023043.2:c.1194A>G | XP_016878532.1:p.Ala398= | |
| NM_005236.3:c.1983A>G MANE Select | NP_005227.1:p.Ala661= |