Canonical Allele Identifier: CA1170023958
Gene: CYP2J2 HGNC NCBI

Linked Data

dbSNP Id: rs1644501006

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59920104G>T , CM000663.2:g.59920104G>T GRCh38
NC_000001.10:g.60385776G>T , CM000663.1:g.60385776G>T GRCh37
NC_000001.9:g.60158364G>T NCBI36
NG_007931.1:g.11648C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371204.4:c.211-4004C>A MANE Select ENSP00000360247.3:n.211-4004C>A
ENST00000468257.2:c.211-4004C>A ENSP00000497807.1:n.211-4004C>A
ENST00000469406.6:c.227-4004C>A ENSP00000497732.1:n.227-4004C>A
ENST00000371204.3:c.211-4004C>A ENSP00000360247.3:n.211-4004C>A
ENST00000466095.5:n.226-4004C>A
ENST00000468257.1:n.236-4004C>A
ENST00000469406.5:n.226-4004C>A
NM_000775.2:c.211-4004C>A NP_000766.2:n.211-4004C>A
XR_246240.2:n.238-4004C>A
XR_946558.1:n.238-4004C>A
NM_000775.3:c.211-4004C>A NP_000766.2:n.211-4004C>A
NR_134981.1:n.263-4004C>A
NR_134982.1:n.263-4004C>A
NM_000775.4:c.211-4004C>A MANE Select NP_000766.2:n.211-4004C>A
NR_134981.2:n.238-4004C>A
NR_134982.2:n.238-4004C>A