Linked Data
ClinVar Variation Id:
1021882
ClinVar RCV Id:
RCV001321720
dbSNP Id:
rs774338870
ExAC:
22:50662847 G / A
gnomAD v2:
22-50662847-G-A
gnomAD v3:
22-50224418-G-A
gnomAD v4:
22-50224418-G-A
COSMIC:
COSM1417046
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50224418G>A , CM000684.2:g.50224418G>A | GRCh38 |
| NC_000022.10:g.50662847G>A , CM000684.1:g.50662847G>A | GRCh37 |
| NC_000022.9:g.49004974G>A | NCBI36 |
| NG_032160.1:g.25554C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248846.10:c.2068C>T MANE Select | ENSP00000248846.5:p.Arg690Trp | |
| ENST00000248846.9:c.2068C>T | ENSP00000248846.5:p.Arg690Trp | |
| ENST00000439308.6:c.2068C>T | ENSP00000397387.2:p.Arg690Trp | |
| ENST00000473946.1:n.377C>T | ||
| ENST00000489511.5:n.85C>T | ||
| ENST00000491449.5:n.375C>T | ||
| ENST00000498611.5:n.2601C>T | ||
| NM_020461.3:c.2068C>T | NP_065194.2:p.Arg690Trp | |
| XR_938347.1:n.2633C>T | ||
| XR_938348.1:n.2633C>T | ||
| XR_001755343.2:n.2637C>T | ||
| XR_001755344.2:n.2637C>T | ||
| XR_002958720.1:n.2637C>T | ||
| XR_938347.2:n.2637C>T | ||
| NM_020461.4:c.2068C>T MANE Select | NP_065194.3:p.Arg690Trp |