Canonical Allele Identifier:
CA476552931
Gene:
MyVariant.info:
GRCh37
chr11:g.101980335C>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102109604C>T , CM000673.2:g.102109604C>T | GRCh38 |
| NC_000011.9:g.101980335C>T , CM000673.1:g.101980335C>T | GRCh37 |
| NC_000011.8:g.101485545C>T | NCBI36 |
| NG_029530.1:g.4144C>T | |
| NG_029530.2:g.4144C>T |