Canonical Allele Identifier: CA1772881290
Gene: EPHX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27557959C= , CM000670.2:g.27557959C= GRCh38
NC_000008.10:g.27415476C= , CM000670.1:g.27415476C= GRCh37
NC_000008.9:g.27471393C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745491.1:n.1647+13715C=