Canonical Allele Identifier: CA1915570313
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.64688715T= , CM000672.2:g.64688715T= GRCh38
NC_000010.10:g.66448472T= , CM000672.1:g.66448472T= GRCh37
NC_000010.9:g.66118478T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946016.1:n.134-2727T=
XR_946017.1:n.83-2727T=