Canonical Allele Identifier: CA1608913607
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169416_8169417delinsCG , CM000668.2:g.8169416_8169417delinsCG GRCh38
NC_000006.11:g.8169649_8169650delinsCG , CM000668.1:g.8169649_8169650delinsCG GRCh37
NC_000006.10:g.8114648_8114649delinsCG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11156_82+11157delinsCG
XR_926441.1:n.189+1496_189+1497delinsCG
XR_926442.1:n.82+11156_82+11157delinsCG
XR_926443.1:n.82+11156_82+11157delinsCG
XR_001743950.1:n.179+1496_179+1497delinsCG
XR_926440.2:n.74+11156_74+11157delinsCG
XR_926441.2:n.179+1496_179+1497delinsCG
XR_926443.2:n.83+11156_83+11157delinsCG