Canonical Allele Identifier: CA2055289530
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293225_93293227delinsGAT , CM000674.2:g.93293225_93293227delinsGAT GRCh38
NC_000012.11:g.93687001_93687003delinsGAT , CM000674.1:g.93687001_93687003delinsGAT GRCh37
NC_000012.10:g.92211132_92211134delinsGAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34800_329+34802delinsATC