Canonical Allele Identifier: CA1608913734
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169522_8169523delinsTC , CM000668.2:g.8169522_8169523delinsTC GRCh38
NC_000006.11:g.8169755_8169756delinsTC , CM000668.1:g.8169755_8169756delinsTC GRCh37
NC_000006.10:g.8114754_8114755delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11262_82+11263delinsTC
XR_926441.1:n.189+1602_189+1603delinsTC
XR_926442.1:n.82+11262_82+11263delinsTC
XR_926443.1:n.82+11262_82+11263delinsTC
XR_001743950.1:n.179+1602_179+1603delinsTC
XR_926440.2:n.74+11262_74+11263delinsTC
XR_926441.2:n.179+1602_179+1603delinsTC
XR_926443.2:n.83+11262_83+11263delinsTC