Canonical Allele Identifier: CA1608913638
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169437T= , CM000668.2:g.8169437T= GRCh38
NC_000006.11:g.8169670T= , CM000668.1:g.8169670T= GRCh37
NC_000006.10:g.8114669T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11177T=
XR_926441.1:n.189+1517T=
XR_926442.1:n.82+11177T=
XR_926443.1:n.82+11177T=
XR_001743950.1:n.179+1517T=
XR_926440.2:n.74+11177T=
XR_926441.2:n.179+1517T=
XR_926443.2:n.83+11177T=