Canonical Allele Identifier: CA2298481283
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477777T= , CM000680.2:g.41477777T= GRCh38
NC_000018.9:g.39057741T= , CM000680.1:g.39057741T= GRCh37
NC_000018.8:g.37311739T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935409.1:n.86-26357T=