Canonical Allele Identifier: CA1932346184
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750689T= , CM000672.2:g.101750689T= GRCh38
NC_000010.10:g.103510446T= , CM000672.1:g.103510446T= GRCh37
NC_000010.9:g.103500436T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946255.1:n.217-6472A=
XR_946255.2:n.217-6472A=