Canonical Allele Identifier: CA10654479
Gene:

Linked Data

ClinVar Variation Id: 368961
ClinVar RCV Id: RCV000392043

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45909655C>T , CM000673.2:g.45909655C>T GRCh38
NC_000011.9:g.45931206C>T , CM000673.1:g.45931206C>T GRCh37
NC_000011.8:g.45887782C>T NCBI36
NG_008460.1:g.13469G>A