Canonical Allele Identifier:
CA204095621
Gene:
MyVariant.info:
GRCh38
chr10:g.20334544A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.20334544A>T , CM000672.2:g.20334544A>T | GRCh38 |
| NC_000010.10:g.20623473A>T , CM000672.1:g.20623473A>T | GRCh37 |
| NC_000010.9:g.20663479A>T | NCBI36 |