Canonical Allele Identifier: CA2293960315
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757050C= , CM000680.2:g.31757050C= GRCh38
NC_000018.9:g.29337013C= , CM000680.1:g.29337013C= GRCh37
NC_000018.8:g.27591011C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5089C=