Canonical Allele Identifier:
CA322337403
Gene:
MyVariant.info:
GRCh38
chr22:g.21628051C>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.21628051C>T , CM000684.2:g.21628051C>T | GRCh38 |
| NC_000022.10:g.21982340C>T , CM000684.1:g.21982340C>T | GRCh37 |
| NC_000022.9:g.20312340C>T | NCBI36 |