Canonical Allele Identifier:
CA242535016
Gene:
MyVariant.info:
GRCh38
chr12:g.102213826A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102213826A>T , CM000674.2:g.102213826A>T | GRCh38 |
| NC_000012.11:g.102607604A>T , CM000674.1:g.102607604A>T | GRCh37 |
| NC_000012.10:g.101131734A>T | NCBI36 |