Canonical Allele Identifier: CA1608914051
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169829C= , CM000668.2:g.8169829C= GRCh38
NC_000006.11:g.8170062C= , CM000668.1:g.8170062C= GRCh37
NC_000006.10:g.8115061C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11569C=
XR_926441.1:n.189+1909C=
XR_926442.1:n.82+11569C=
XR_926443.1:n.82+11569C=
XR_001743950.1:n.179+1909C=
XR_926440.2:n.74+11569C=
XR_926441.2:n.179+1909C=
XR_926443.2:n.83+11569C=