Canonical Allele Identifier: CA13430008
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 548114
dbSNP Id: rs662799

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116792991G>A , CM000673.2:g.116792991G>A GRCh38
NC_000011.9:g.116663707G>A , CM000673.1:g.116663707G>A GRCh37
NC_000011.8:g.116168917G>A NCBI36
NG_015894.1:g.4430C>T