Canonical Allele Identifier: CA1608913721
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169510C= , CM000668.2:g.8169510C= GRCh38
NC_000006.11:g.8169743C= , CM000668.1:g.8169743C= GRCh37
NC_000006.10:g.8114742C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11250C=
XR_926441.1:n.189+1590C=
XR_926442.1:n.82+11250C=
XR_926443.1:n.82+11250C=
XR_001743950.1:n.179+1590C=
XR_926440.2:n.74+11250C=
XR_926441.2:n.179+1590C=
XR_926443.2:n.83+11250C=