Canonical Allele Identifier: CA1772926138
Gene: EPHX2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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