Canonical Allele Identifier: CA2221608945
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50109036_50109037delinsCT , CM000678.2:g.50109036_50109037delinsCT GRCh38
NC_000016.9:g.50142947_50142948delinsCT , CM000678.1:g.50142947_50142948delinsCT GRCh37
NC_000016.8:g.48700448_48700449delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011523490.1:c.115-2385_115-2384delinsAG XP_011521792.1:n.115-2385_115-2384delinsAG