Canonical Allele Identifier:
CA495615710
Gene:
MyVariant.info:
GRCh37
chr16:g.56991265C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56957353C>A , CM000678.2:g.56957353C>A | GRCh38 |
| NC_000016.9:g.56991265C>A , CM000678.1:g.56991265C>A | GRCh37 |
| NC_000016.8:g.55548766C>A | NCBI36 |
| NG_008952.1:g.431C>A |