Canonical Allele Identifier:
CA317824449
Gene:
MyVariant.info:
GRCh38
chr21:g.14472698G>T
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.14472698G>T , CM000683.2:g.14472698G>T | GRCh38 |
| NC_000021.8:g.15845019G>T , CM000683.1:g.15845019G>T | GRCh37 |
| NC_000021.7:g.14766890G>T | NCBI36 |