Canonical Allele Identifier:
CA13427637
Gene:
Linked Data
ClinVar Variation Id:
1166185
ClinVar RCV Id:
RCV001514053
gnomAD v2:
11-102826539-C-T
gnomAD v3:
11-102955810-C-T
gnomAD v4:
11-102955810-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102955810C>T , CM000673.2:g.102955810C>T | GRCh38 |
| NC_000011.9:g.102826539C>T , CM000673.1:g.102826539C>T | GRCh37 |
| NC_000011.8:g.102331749C>T | NCBI36 |
| NG_021404.1:g.4925G>A |