Canonical Allele Identifier: CA910080477
Gene:

Linked Data

dbSNP Id: rs56217453

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266868_72266871dup , CM000665.2:g.72266868_72266871dup GRCh38
NC_000003.11:g.72316019_72316022dup , CM000665.1:g.72316019_72316022dup GRCh37
NC_000003.10:g.72398709_72398712dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8285_835+8288dup