Canonical Allele Identifier:
CA249778225
Gene:
MyVariant.info:
GRCh38
chr13:g.47588423C>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.47588423C>T , CM000675.2:g.47588423C>T | GRCh38 |
| NC_000013.10:g.48162558C>T , CM000675.1:g.48162558C>T | GRCh37 |
| NC_000013.9:g.47060559C>T | NCBI36 |