Canonical Allele Identifier: CA1170023931
Gene: CYP2J2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59920092C= , CM000663.2:g.59920092C= GRCh38
NC_000001.10:g.60385764C= , CM000663.1:g.60385764C= GRCh37
NC_000001.9:g.60158352C= NCBI36
NG_007931.1:g.11660G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371204.4:c.211-3992G= MANE Select ENSP00000360247.3:n.211-3992G=
ENST00000468257.2:c.211-3992G= ENSP00000497807.1:n.211-3992G=
ENST00000469406.6:c.227-3992G= ENSP00000497732.1:n.227-3992G=
ENST00000371204.3:c.211-3992G= ENSP00000360247.3:n.211-3992G=
ENST00000466095.5:n.226-3992G=
ENST00000468257.1:n.236-3992G=
ENST00000469406.5:n.226-3992G=
NM_000775.2:c.211-3992G= NP_000766.2:n.211-3992G=
XR_246240.2:n.238-3992G=
XR_946558.1:n.238-3992G=
NM_000775.3:c.211-3992G= NP_000766.2:n.211-3992G=
NR_134981.1:n.263-3992G=
NR_134982.1:n.263-3992G=
NM_000775.4:c.211-3992G= MANE Select NP_000766.2:n.211-3992G=
NR_134981.2:n.238-3992G=
NR_134982.2:n.238-3992G=