Canonical Allele Identifier: CA1140266005
Gene: CYP2J2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59896030A= , CM000663.2:g.59896030A= GRCh38
NC_000001.10:g.60361702A= , CM000663.1:g.60361702A= GRCh37
NC_000001.9:g.60134290A= NCBI36
NG_007931.1:g.35722T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371204.4:c.1331-2201T= MANE Select ENSP00000360247.3:n.1331-2201T=
ENST00000468257.2:c.*273-2201T= ENSP00000497807.1:n.*273-2201T=
ENST00000469406.6:c.*1243-2201T= ENSP00000497732.1:n.*1243-2201T=
ENST00000371204.3:c.1331-2201T= ENSP00000360247.3:n.1331-2201T=
ENST00000466095.5:n.1158-2201T=
ENST00000469406.5:n.1497-2201T=
ENST00000492633.5:n.2036-2201T=
NM_000775.2:c.1331-2201T= NP_000766.2:n.1331-2201T=
XR_246240.2:n.1170-2201T=
XR_946558.1:n.1509-2201T=
NM_000775.3:c.1331-2201T= NP_000766.2:n.1331-2201T=
NR_134981.1:n.1195-2201T=
NR_134982.1:n.1534-2201T=
NM_000775.4:c.1331-2201T= MANE Select NP_000766.2:n.1331-2201T=
NR_134981.2:n.1170-2201T=
NR_134982.2:n.1509-2201T=