Canonical Allele Identifier:
CA266826348
Gene:
Linked Data
dbSNP Id:
rs10129255
gnomAD v3:
14-106767970-C-T
gnomAD v4:
14-106767970-C-T
MyVariant Identifiers:
chr14:g.106767970C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.106767970C>T , CM000676.2:g.106767970C>T | GRCh38 |