Canonical Allele Identifier: CA1608913751
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169536C= , CM000668.2:g.8169536C= GRCh38
NC_000006.11:g.8169769C= , CM000668.1:g.8169769C= GRCh37
NC_000006.10:g.8114768C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926440.1:n.82+11276C=
XR_926441.1:n.189+1616C=
XR_926442.1:n.82+11276C=
XR_926443.1:n.82+11276C=
XR_001743950.1:n.179+1616C=
XR_926440.2:n.74+11276C=
XR_926441.2:n.179+1616C=
XR_926443.2:n.83+11276C=