Canonical Allele Identifier:
CA181172505
Gene:
MyVariant.info:
GRCh38
chr8:g.83078996A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.83078996A>T , CM000670.2:g.83078996A>T | GRCh38 |
| NC_000008.10:g.83991231A>T , CM000670.1:g.83991231A>T | GRCh37 |
| NC_000008.9:g.84153786A>T | NCBI36 |