Canonical Allele Identifier: CA1002239182

Gene: CYP2J2

Linked Data

• dbSNP Id: rs1644499853
• gnomAD v3: 1-59920034-GT-G
• gnomAD v4: 1-59920034-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59920035del , CM000663.2:g.59920035del	GRCh38
NC_000001.10:g.60385707del , CM000663.1:g.60385707del	GRCh37
NC_000001.9:g.60158295del	NCBI36
NG_007931.1:g.11717del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-3935del MANE Select	ENSP00000360247.3:n.211-3935del
ENST00000468257.2:c.211-3935del	ENSP00000497807.1:n.211-3935del
ENST00000469406.6:c.227-3935del	ENSP00000497732.1:n.227-3935del
ENST00000371204.3:c.211-3935del	ENSP00000360247.3:n.211-3935del
ENST00000466095.5:n.226-3935del
ENST00000468257.1:n.236-3935del
ENST00000469406.5:n.226-3935del
NM_000775.2:c.211-3935del	NP_000766.2:n.211-3935del
XR_246240.2:n.238-3935del
XR_946558.1:n.238-3935del
NM_000775.3:c.211-3935del	NP_000766.2:n.211-3935del
NR_134981.1:n.263-3935del
NR_134982.1:n.263-3935del
NM_000775.4:c.211-3935del MANE Select	NP_000766.2:n.211-3935del
NR_134981.2:n.238-3935del
NR_134982.2:n.238-3935del