Canonical Allele Identifier:
CA476552930
Gene:
MyVariant.info:
GRCh37
chr11:g.101980335C>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102109604C>G , CM000673.2:g.102109604C>G | GRCh38 |
| NC_000011.9:g.101980335C>G , CM000673.1:g.101980335C>G | GRCh37 |
| NC_000011.8:g.101485545C>G | NCBI36 |
| NG_029530.1:g.4144C>G | |
| NG_029530.2:g.4144C>G |