Canonical Allele Identifier: CA1772881928
Gene: EPHX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27559284G= , CM000670.2:g.27559284G= GRCh38
NC_000008.10:g.27416801G= , CM000670.1:g.27416801G= GRCh37
NC_000008.9:g.27472718G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745491.1:n.1647+15040G=