Canonical Allele Identifier:
CA321756036
Gene:
MyVariant.info:
GRCh38
chr21:g.44241460C>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44241460C>T , CM000683.2:g.44241460C>T | GRCh38 |