Canonical Allele Identifier: CA2072411499
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529607_131529608delinsAG , CM000674.2:g.131529607_131529608delinsAG GRCh38
NC_000012.11:g.132014152_132014153delinsAG , CM000674.1:g.132014152_132014153delinsAG GRCh37
NC_000012.10:g.130580105_130580106delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+167_1076+168delinsCT
XR_001749407.2:n.1067+167_1067+168delinsCT