Canonical Allele Identifier: CA1170013597
Gene: CYP2J2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59896477T= , CM000663.2:g.59896477T= GRCh38
NC_000001.10:g.60362149T= , CM000663.1:g.60362149T= GRCh37
NC_000001.9:g.60134737T= NCBI36
NG_007931.1:g.35275A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371204.4:c.1331-2648A= MANE Select ENSP00000360247.3:n.1331-2648A=
ENST00000468257.2:c.*273-2648A= ENSP00000497807.1:n.*273-2648A=
ENST00000469406.6:c.*1243-2648A= ENSP00000497732.1:n.*1243-2648A=
ENST00000371204.3:c.1331-2648A= ENSP00000360247.3:n.1331-2648A=
ENST00000466095.5:n.1158-2648A=
ENST00000469406.5:n.1497-2648A=
ENST00000492633.5:n.2036-2648A=
NM_000775.2:c.1331-2648A= NP_000766.2:n.1331-2648A=
XR_246240.2:n.1170-2648A=
XR_946558.1:n.1509-2648A=
NM_000775.3:c.1331-2648A= NP_000766.2:n.1331-2648A=
NR_134981.1:n.1195-2648A=
NR_134982.1:n.1534-2648A=
NM_000775.4:c.1331-2648A= MANE Select NP_000766.2:n.1331-2648A=
NR_134981.2:n.1170-2648A=
NR_134982.2:n.1509-2648A=