Canonical Allele Identifier: CA2293960312
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757039T= , CM000680.2:g.31757039T= GRCh38
NC_000018.9:g.29337002T= , CM000680.1:g.29337002T= GRCh37
NC_000018.8:g.27591000T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5100T=