Canonical Allele Identifier: CA13471613
Gene:

Linked Data

ClinVar Variation Id: 1286349
ClinVar RCV Id: RCV001710131
dbSNP Id: rs5081

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116835630A>T , CM000673.2:g.116835630A>T GRCh38
NC_000011.9:g.116706346A>T , CM000673.1:g.116706346A>T GRCh37
NC_000011.8:g.116211556A>T NCBI36
NG_012021.1:g.6993T>A , LRG_767:g.6993T>A