Canonical Allele Identifier: CA2072411476
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529553_131529556delinsCTAT , CM000674.2:g.131529553_131529556delinsCTAT GRCh38
NC_000012.11:g.132014098_132014101delinsCTAT , CM000674.1:g.132014098_132014101delinsCTAT GRCh37
NC_000012.10:g.130580051_130580054delinsCTAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+219_1076+222delinsATAG
XR_001749407.2:n.1067+219_1067+222delinsATAG