Canonical Allele Identifier:
CA276904847
Gene:
Linked Data
ClinVar Variation Id:
675625
dbSNP Id:
rs11466013
gnomAD v2:
16-3306917-C-T
gnomAD v3:
16-3256917-C-T
gnomAD v4:
16-3256917-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3256917C>T , CM000678.2:g.3256917C>T | GRCh38 |
| NC_000016.9:g.3306917C>T , CM000678.1:g.3306917C>T | GRCh37 |
| NC_000016.8:g.3246918C>T | NCBI36 |
| NG_007871.1:g.4711G>A , LRG_190:g.4711G>A |