Canonical Allele Identifier:
CA315659586
Gene:
MyVariant.info:
GRCh38
chr20:g.46134645C>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46134645C>A , CM000682.2:g.46134645C>A | GRCh38 |
| NC_000020.10:g.44763284C>A , CM000682.1:g.44763284C>A | GRCh37 |
| NC_000020.9:g.44196691C>A | NCBI36 |