Canonical Allele Identifier: CA1772925715
Community Standard Title: NC_000008.11:g.27595330G=
Gene: EPHX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27595330G= , CM000670.2:g.27595330G= GRCh38
NC_000008.10:g.27452847G= , CM000670.1:g.27452847G= GRCh37
NC_000008.9:g.27508764G= NCBI36
NG_027845.1:g.24481C=

Transcript Alleles

HGVS Amino-acid Change
XR_001745491.1:n.1928-1737G=
XR_949609.1:n.3190-1737G=
XR_949610.1:n.2503-1737G=
XR_949611.1:n.3149-1737G=