Canonical Allele Identifier:
CA324987626
Gene:
MyVariant.info:
GRCh38
chr22:g.44572650G>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.44572650G>T , CM000684.2:g.44572650G>T | GRCh38 |
| NC_000022.10:g.44968530G>T , CM000684.1:g.44968530G>T | GRCh37 |
| NC_000022.9:g.43347194G>T | NCBI36 |