Canonical Allele Identifier: CA123811
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 14207
dbSNP Id: rs1024611

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34252769A>G , CM000679.2:g.34252769A>G GRCh38
NC_000017.10:g.32579788A>G , CM000679.1:g.32579788A>G GRCh37
NC_000017.9:g.29603901A>G NCBI36
NG_012123.1:g.2493A>G