Canonical Allele Identifier: CA2298481303
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477812G= , CM000680.2:g.41477812G= GRCh38
NC_000018.9:g.39057776G= , CM000680.1:g.39057776G= GRCh37
NC_000018.8:g.37311774G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935409.1:n.86-26322G=