Canonical Allele Identifier: CA1932346137
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750660C= , CM000672.2:g.101750660C= GRCh38
NC_000010.10:g.103510417C= , CM000672.1:g.103510417C= GRCh37
NC_000010.9:g.103500407C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946255.1:n.217-6443G=
XR_946255.2:n.217-6443G=