Canonical Allele Identifier:
CA229440451
Gene:
dbSNP:
MyVariant.info:
GRCh38
chr11:g.117880025C>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.117880025C>T , CM000673.2:g.117880025C>T | GRCh38 |
| NC_000011.9:g.117750740C>T , CM000673.1:g.117750740C>T | GRCh37 |
| NC_000011.8:g.117255950C>T | NCBI36 |
| NG_013071.1:g.2406G>A |