Canonical Allele Identifier: CA1170023744
Gene: CYP2J2 HGNC NCBI

Linked Data

dbSNP Id: rs1644498772

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59919876T>C , CM000663.2:g.59919876T>C GRCh38
NC_000001.10:g.60385548T>C , CM000663.1:g.60385548T>C GRCh37
NC_000001.9:g.60158136T>C NCBI36
NG_007931.1:g.11876A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371204.4:c.211-3776A>G MANE Select ENSP00000360247.3:n.211-3776A>G
ENST00000468257.2:c.211-3776A>G ENSP00000497807.1:n.211-3776A>G
ENST00000469406.6:c.227-3776A>G ENSP00000497732.1:n.227-3776A>G
ENST00000371204.3:c.211-3776A>G ENSP00000360247.3:n.211-3776A>G
ENST00000466095.5:n.226-3776A>G
ENST00000468257.1:n.236-3776A>G
ENST00000469406.5:n.226-3776A>G
NM_000775.2:c.211-3776A>G NP_000766.2:n.211-3776A>G
XR_246240.2:n.238-3776A>G
XR_946558.1:n.238-3776A>G
NM_000775.3:c.211-3776A>G NP_000766.2:n.211-3776A>G
NR_134981.1:n.263-3776A>G
NR_134982.1:n.263-3776A>G
NM_000775.4:c.211-3776A>G MANE Select NP_000766.2:n.211-3776A>G
NR_134981.2:n.238-3776A>G
NR_134982.2:n.238-3776A>G