Canonical Allele Identifier: CA1170023739
Gene: CYP2J2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59922920T= , CM000663.2:g.59922920T= GRCh38
NC_000001.10:g.60388592T= , CM000663.1:g.60388592T= GRCh37
NC_000001.9:g.60161180T= NCBI36
NG_007931.1:g.8832A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371204.4:c.210+3617A= MANE Select ENSP00000360247.3:n.210+3617A=
ENST00000468257.2:c.210+3617A= ENSP00000497807.1:n.210+3617A=
ENST00000469406.6:c.226+3601A= ENSP00000497732.1:n.226+3601A=
ENST00000371204.3:c.210+3617A= ENSP00000360247.3:n.210+3617A=
ENST00000466095.5:n.225+3617A=
ENST00000468257.1:n.235+3601A=
ENST00000469406.5:n.225+3617A=
NM_000775.2:c.210+3617A= NP_000766.2:n.210+3617A=
XR_246240.2:n.237+3617A=
XR_946558.1:n.237+3617A=
NM_000775.3:c.210+3617A= NP_000766.2:n.210+3617A=
NR_134981.1:n.262+3617A=
NR_134982.1:n.262+3617A=
NM_000775.4:c.210+3617A= MANE Select NP_000766.2:n.210+3617A=
NR_134981.2:n.237+3617A=
NR_134982.2:n.237+3617A=