Canonical Allele Identifier: CA2001592057
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.114360671_114360674delinsCAAT , CM000673.2:g.114360671_114360674delinsCAAT GRCh38
NC_000011.9:g.114231393_114231396delinsCAAT , CM000673.1:g.114231393_114231396delinsCAAT GRCh37
NC_000011.8:g.113736603_113736606delinsCAAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120567.1:n.3792_3795delinsATTG