Canonical Allele Identifier:
CA77255903
Gene:
MyVariant.info:
GRCh38
chr3:g.72343990G>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.72343990G>A , CM000665.2:g.72343990G>A | GRCh38 |
| NC_000003.11:g.72393141G>A , CM000665.1:g.72393141G>A | GRCh37 |
| NC_000003.10:g.72475831G>A | NCBI36 |