Canonical Allele Identifier: CA370804669

Gene: EPHX2

Linked Data

• MyVariant Identifiers: chr8:g.27358480G>C (hg19) ; chr8:g.27500963G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27500963G>C , CM000670.2:g.27500963G>C	GRCh38
NC_000008.10:g.27358480G>C , CM000670.1:g.27358480G>C	GRCh37
NC_000008.9:g.27414397G>C	NCBI36
NG_012064.1:g.14836G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521400.6:c.139G>C MANE Select	ENSP00000430269.1:p.Glu47Gln
ENST00000380476.7:c.-20-1G>C	ENSP00000369843.3:n.-20-1G>C
ENST00000517536.5:c.139G>C	ENSP00000428875.1:p.Glu47Gln
ENST00000518328.5:c.139G>C	ENSP00000430779.1:p.Glu47Gln
ENST00000518379.5:c.139G>C	ENSP00000427956.1:p.Glu47Gln
ENST00000520623.5:n.223G>C
ENST00000520666.1:n.151G>C
ENST00000521400.5:c.139G>C	ENSP00000430269.1:p.Glu47Gln
ENST00000521684.1:c.138G>C
ENST00000521780.5:c.-12-2641G>C	ENSP00000430302.1:n.-12-2641G>C
ENST00000523827.1:n.362G>C
NM_001256482.1:c.-20-1G>C	NP_001243411.1:n.-20-1G>C
NM_001256483.1:c.-12-2641G>C	NP_001243412.1:n.-12-2641G>C
NM_001256484.1:c.-21G>C	NP_001243413.1:n.-21G>C
NM_001979.5:c.139G>C	NP_001970.2:p.Glu47Gln
XM_017013199.1:c.139G>C	XP_016868688.1:p.Glu47Gln
XM_017013200.1:c.139G>C	XP_016868689.1:p.Glu47Gln
XR_001745491.1:n.197G>C
NM_001256482.2:c.-20-1G>C	NP_001243411.1:n.-20-1G>C
NM_001256483.2:c.-12-2641G>C	NP_001243412.1:n.-12-2641G>C
NM_001256484.2:c.-21G>C	NP_001243413.1:n.-21G>C
NM_001979.6:c.139G>C MANE Select	NP_001970.2:p.Glu47Gln