Canonical Allele Identifier: CA1140187662
Gene: CYP2J2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59923002G= , CM000663.2:g.59923002G= GRCh38
NC_000001.10:g.60388674G= , CM000663.1:g.60388674G= GRCh37
NC_000001.9:g.60161262G= NCBI36
NG_007931.1:g.8750C=

Transcript Alleles

HGVS Amino-acid Change
NM_000775.4:c.210+3535C= MANE Select NP_000766.2:n.210+3535C=
ENST00000371204.4:c.210+3535C= MANE Select ENSP00000360247.3:n.210+3535C=
NM_000775.2:c.210+3535C= NP_000766.2:n.210+3535C=
NM_000775.3:c.210+3535C= NP_000766.2:n.210+3535C=
NR_134981.1:n.262+3535C=
NR_134981.2:n.237+3535C=
NR_134982.1:n.262+3535C=
NR_134982.2:n.237+3535C=
ENST00000371204.3:c.210+3535C= ENSP00000360247.3:n.210+3535C=
ENST00000466095.5:n.225+3535C=
ENST00000468257.1:n.235+3519C=
ENST00000468257.2:c.210+3535C= ENSP00000497807.1:n.210+3535C=
ENST00000469406.5:n.225+3535C=
ENST00000469406.6:c.226+3519C= ENSP00000497732.1:n.226+3519C=
XR_246240.2:n.237+3535C=
XR_946558.1:n.237+3535C=