Canonical Allele Identifier:
CA219859581
Gene:
MyVariant.info:
GRCh38
chr11:g.27731216T>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.27731216T>G , CM000673.2:g.27731216T>G | GRCh38 |
| NC_000011.9:g.27752763T>G , CM000673.1:g.27752763T>G | GRCh37 |
| NC_000011.8:g.27709339T>G | NCBI36 |