Canonical Allele Identifier: CA2298481261
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477723T= , CM000680.2:g.41477723T= GRCh38
NC_000018.9:g.39057687T= , CM000680.1:g.39057687T= GRCh37
NC_000018.8:g.37311685T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935409.1:n.86-26411T=