Canonical Allele Identifier: CA2302316835
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645946A= , CM000680.2:g.49645946A= GRCh38
NC_000018.9:g.47172316A= , CM000680.1:g.47172316A= GRCh37
NC_000018.8:g.45426314A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935461.1:n.162-16088A=
XR_001753446.1:n.898-16088A=