Canonical Allele Identifier: CA1002239124

Gene: CYP2J2

Linked Data

• gnomAD v3: 1-59919878-AGATGCT-A
• gnomAD v4: 1-59919878-AGATGCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59919879_59919884del , CM000663.2:g.59919879_59919884del	GRCh38
NC_000001.10:g.60385551_60385556del , CM000663.1:g.60385551_60385556del	GRCh37
NC_000001.9:g.60158139_60158144del	NCBI36
NG_007931.1:g.11868_11873del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-3784_211-3779del MANE Select	ENSP00000360247.3:n.211-3784_211-3779del
ENST00000468257.2:c.211-3784_211-3779del	ENSP00000497807.1:n.211-3784_211-3779del
ENST00000469406.6:c.227-3784_227-3779del	ENSP00000497732.1:n.227-3784_227-3779del
ENST00000371204.3:c.211-3784_211-3779del	ENSP00000360247.3:n.211-3784_211-3779del
ENST00000466095.5:n.226-3784_226-3779del
ENST00000468257.1:n.236-3784_236-3779del
ENST00000469406.5:n.226-3784_226-3779del
NM_000775.2:c.211-3784_211-3779del	NP_000766.2:n.211-3784_211-3779del
XR_246240.2:n.238-3784_238-3779del
XR_946558.1:n.238-3784_238-3779del
NM_000775.3:c.211-3784_211-3779del	NP_000766.2:n.211-3784_211-3779del
NR_134981.1:n.263-3784_263-3779del
NR_134982.1:n.263-3784_263-3779del
NM_000775.4:c.211-3784_211-3779del MANE Select	NP_000766.2:n.211-3784_211-3779del
NR_134981.2:n.238-3784_238-3779del
NR_134982.2:n.238-3784_238-3779del