Canonical Allele Identifier: CA73933666
Gene:

Linked Data

ClinVar Variation Id: 1273880
ClinVar RCV Id: RCV001684868

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467792_48467796dup , CM000665.2:g.48467792_48467796dup GRCh38
NC_000003.11:g.48509191_48509195dup , CM000665.1:g.48509191_48509195dup GRCh37
NC_000003.10:g.48484195_48484199dup NCBI36
NG_009820.1:g.6963_6967dup
NG_033100.1:g.38066_38070dup
NG_009820.2:g.6963_6967dup