Linked Data
ClinVar Variation Id:
1903366
ClinVar RCV Id:
RCV002586288
dbSNP Id:
rs199577822
gnomAD v4:
22-50220572-G-A
COSMIC:
COSM1417041
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50220572G>A , CM000684.2:g.50220572G>A | GRCh38 |
| NC_000022.10:g.50659001G>A , CM000684.1:g.50659001G>A | GRCh37 |
| NC_000022.9:g.49001128G>A | NCBI36 |
| NG_032160.1:g.29400C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248846.10:c.3787C>T MANE Select | ENSP00000248846.5:p.Arg1263Trp | |
| ENST00000248846.9:c.3787C>T | ENSP00000248846.5:p.Arg1263Trp | |
| ENST00000439308.6:c.3787C>T | ENSP00000397387.2:p.Arg1263Trp | |
| ENST00000491449.5:n.2094C>T | ||
| ENST00000498611.5:n.3618-557C>T | ||
| NM_020461.3:c.3787C>T | NP_065194.2:p.Arg1263Trp | |
| XR_938347.1:n.4352C>T | ||
| XR_938348.1:n.3050-557C>T | ||
| XR_001755343.2:n.4356C>T | ||
| XR_001755344.2:n.4356C>T | ||
| XR_002958720.1:n.3054-557C>T | ||
| XR_938347.2:n.4356C>T | ||
| NM_020461.4:c.3787C>T MANE Select | NP_065194.3:p.Arg1263Trp |