Canonical Allele Identifier: CA2302316767
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645820T= , CM000680.2:g.49645820T= GRCh38
NC_000018.9:g.47172190T= , CM000680.1:g.47172190T= GRCh37
NC_000018.8:g.45426188T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935461.1:n.162-16214T=
XR_001753446.1:n.898-16214T=