Linked Data
ClinVar Variation Id:
498579
ClinVar RCV Id:
RCV000593062
dbSNP Id:
rs1368309193
gnomAD v2:
21-47417661-G-A
gnomAD v4:
21-45997747-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45997747G>A , CM000683.2:g.45997747G>A | GRCh38 |
| NC_000021.8:g.47417661G>A , CM000683.1:g.47417661G>A | GRCh37 |
| NC_000021.7:g.46242089G>A | NCBI36 |
| NG_008674.1:g.20999G>A , LRG_475:g.20999G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683550.1:n.284G>A | ||
| ENST00000361866.8:c.1509G>A MANE Select | ENSP00000355180.3:p.Gly503= | |
| ENST00000361866.7:c.1509G>A | ENSP00000355180.3:p.Gly503= | |
| ENST00000612273.1:c.1509G>A | ENSP00000483630.1:p.Gly503= | |
| NM_001848.2:c.1509G>A , LRG_475t1:c.1509G>A | NP_001839.2:p.Gly503= | |
| NM_001848.3:c.1509G>A MANE Select | NP_001839.2:p.Gly503= |