Canonical Allele Identifier: CA1608913873
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169654A= , CM000668.2:g.8169654A= GRCh38
NC_000006.11:g.8169887A= , CM000668.1:g.8169887A= GRCh37
NC_000006.10:g.8114886A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11394A=
XR_926441.1:n.189+1734A=
XR_926442.1:n.82+11394A=
XR_926443.1:n.82+11394A=
XR_001743950.1:n.179+1734A=
XR_926440.2:n.74+11394A=
XR_926441.2:n.179+1734A=
XR_926443.2:n.83+11394A=