Canonical Allele Identifier:
CA334645884
Gene:
Linked Data
ClinVar Variation Id:
1318441
ClinVar RCV Id:
RCV001753216
dbSNP Id:
rs3813928
gnomAD v2:
X-113818282-G-A
gnomAD v3:
X-114583809-G-A
gnomAD v4:
X-114583809-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.114583809G>A , CM000685.2:g.114583809G>A | GRCh38 |
| NC_000023.10:g.113818282G>A , CM000685.1:g.113818282G>A | GRCh37 |
| NC_000023.9:g.113724538G>A | NCBI36 |
| NG_012082.2:g.4725G>A | |
| NG_012082.3:g.4725G>A |