Canonical Allele Identifier:
CA191256935
Gene:
MyVariant.info:
GRCh38
chr9:g.22134173C>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22134173C>A , CM000671.2:g.22134173C>A | GRCh38 |
| NC_000009.11:g.22134172C>A , CM000671.1:g.22134172C>A | GRCh37 |
| NC_000009.10:g.22124172C>A | NCBI36 |