Canonical Allele Identifier: CA13443703
Gene:

Linked Data

ClinVar Variation Id: 1240658
ClinVar RCV Id: RCV001641046
dbSNP Id: rs36211089

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67583533C>T , CM000673.2:g.67583533C>T GRCh38
NC_000011.9:g.67351004C>T , CM000673.1:g.67351004C>T GRCh37
NC_000011.8:g.67107580C>T NCBI36
NG_012075.1:g.4939C>T , LRG_723:g.4939C>T