Canonical Allele Identifier:
CA208612817
Gene:
MyVariant.info:
GRCh38
chr10:g.62710915C>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.62710915C>A , CM000672.2:g.62710915C>A | GRCh38 |
| NC_000010.10:g.64470675C>A , CM000672.1:g.64470675C>A | GRCh37 |
| NC_000010.9:g.64140681C>A | NCBI36 |