Canonical Allele Identifier: CA1772926137
Gene: EPHX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27596246C= , CM000670.2:g.27596246C= GRCh38
NC_000008.10:g.27453763C= , CM000670.1:g.27453763C= GRCh37
NC_000008.9:g.27509680C= NCBI36
NG_027845.1:g.23565G=

Transcript Alleles

HGVS Amino-acid Change
XR_949609.1:n.3190-821C=
XR_949610.1:n.2503-821C=
XR_949611.1:n.3149-821C=
XR_001745491.1:n.1928-821C=