Canonical Allele Identifier: CA1689218143
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400602_13400606delinsCAAAT , CM000669.2:g.13400602_13400606delinsCAAAT GRCh38
NC_000007.13:g.13440227_13440231delinsCAAAT , CM000669.1:g.13440227_13440231delinsCAAAT GRCh37
NC_000007.12:g.13406752_13406756delinsCAAAT NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745097.1:n.147+90279_147+90283delinsCAAAT