Linked Data
ClinVar Variation Id:
1379158
ClinVar RCV Id:
RCV001914781
dbSNP Id:
rs779620115
ExAC:
22:50659562 G / A
gnomAD v2:
22-50659562-G-A
gnomAD v3:
22-50221133-G-A
gnomAD v4:
22-50221133-G-A
COSMIC:
COSM4746377
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50221133G>A , CM000684.2:g.50221133G>A | GRCh38 |
| NC_000022.10:g.50659562G>A , CM000684.1:g.50659562G>A | GRCh37 |
| NC_000022.9:g.49001689G>A | NCBI36 |
| NG_032160.1:g.28839C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248846.10:c.3226C>T MANE Select | ENSP00000248846.5:p.Arg1076Trp | |
| ENST00000248846.9:c.3226C>T | ENSP00000248846.5:p.Arg1076Trp | |
| ENST00000439308.6:c.3226C>T | ENSP00000397387.2:p.Arg1076Trp | |
| ENST00000491449.5:n.1533C>T | ||
| ENST00000498611.5:n.3617+142C>T | ||
| NM_020461.3:c.3226C>T | NP_065194.2:p.Arg1076Trp | |
| XR_938347.1:n.3791C>T | ||
| XR_938348.1:n.3049+895C>T | ||
| XR_001755343.2:n.3795C>T | ||
| XR_001755344.2:n.3795C>T | ||
| XR_002958720.1:n.3053+895C>T | ||
| XR_938347.2:n.3795C>T | ||
| NM_020461.4:c.3226C>T MANE Select | NP_065194.3:p.Arg1076Trp |