Canonical Allele Identifier: CA1170023967
Gene: CYP2J2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59920129T= , CM000663.2:g.59920129T= GRCh38
NC_000001.10:g.60385801T= , CM000663.1:g.60385801T= GRCh37
NC_000001.9:g.60158389T= NCBI36
NG_007931.1:g.11623A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371204.4:c.211-4029A= MANE Select ENSP00000360247.3:n.211-4029A=
ENST00000468257.2:c.211-4029A= ENSP00000497807.1:n.211-4029A=
ENST00000469406.6:c.227-4029A= ENSP00000497732.1:n.227-4029A=
ENST00000371204.3:c.211-4029A= ENSP00000360247.3:n.211-4029A=
ENST00000466095.5:n.226-4029A=
ENST00000468257.1:n.236-4029A=
ENST00000469406.5:n.226-4029A=
NM_000775.2:c.211-4029A= NP_000766.2:n.211-4029A=
XR_246240.2:n.238-4029A=
XR_946558.1:n.238-4029A=
NM_000775.3:c.211-4029A= NP_000766.2:n.211-4029A=
NR_134981.1:n.263-4029A=
NR_134982.1:n.263-4029A=
NM_000775.4:c.211-4029A= MANE Select NP_000766.2:n.211-4029A=
NR_134981.2:n.238-4029A=
NR_134982.2:n.238-4029A=