Canonical Allele Identifier:
CA266837858
Gene:
Linked Data
dbSNP Id:
rs12590667
gnomAD v3:
14-106779223-C-T
gnomAD v4:
14-106779223-C-T
MyVariant Identifiers:
chr14:g.106779223C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.106779223C>T , CM000676.2:g.106779223C>T | GRCh38 |
| NC_000014.7:g.106258507C>T | NCBI36 |