Canonical Allele Identifier:
CA189033325
Gene:
MyVariant.info:
GRCh38
chr9:g.7682601C>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.7682601C>G , CM000671.2:g.7682601C>G | GRCh38 |
| NC_000009.11:g.7682601C>G , CM000671.1:g.7682601C>G | GRCh37 |
| NC_000009.10:g.7672601C>G | NCBI36 |