Canonical Allele Identifier: CA1932346168
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750685A= , CM000672.2:g.101750685A= GRCh38
NC_000010.10:g.103510442A= , CM000672.1:g.103510442A= GRCh37
NC_000010.9:g.103500432A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946255.1:n.217-6468T=
XR_946255.2:n.217-6468T=