Canonical Allele Identifier: CA1002239094

Gene: CYP2J2

Linked Data

• gnomAD v3: 1-59919865-ACAGG-A
• gnomAD v4: 1-59919865-ACAGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59919867_59919870del , CM000663.2:g.59919867_59919870del	GRCh38
NC_000001.10:g.60385539_60385542del , CM000663.1:g.60385539_60385542del	GRCh37
NC_000001.9:g.60158127_60158130del	NCBI36
NG_007931.1:g.11883_11886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-3769_211-3766del MANE Select	ENSP00000360247.3:n.211-3769_211-3766del
ENST00000468257.2:c.211-3769_211-3766del	ENSP00000497807.1:n.211-3769_211-3766del
ENST00000469406.6:c.227-3769_227-3766del	ENSP00000497732.1:n.227-3769_227-3766del
ENST00000371204.3:c.211-3769_211-3766del	ENSP00000360247.3:n.211-3769_211-3766del
ENST00000466095.5:n.226-3769_226-3766del
ENST00000468257.1:n.236-3769_236-3766del
ENST00000469406.5:n.226-3769_226-3766del
NM_000775.2:c.211-3769_211-3766del	NP_000766.2:n.211-3769_211-3766del
XR_246240.2:n.238-3769_238-3766del
XR_946558.1:n.238-3769_238-3766del
NM_000775.3:c.211-3769_211-3766del	NP_000766.2:n.211-3769_211-3766del
NR_134981.1:n.263-3769_263-3766del
NR_134982.1:n.263-3769_263-3766del
NM_000775.4:c.211-3769_211-3766del MANE Select	NP_000766.2:n.211-3769_211-3766del
NR_134981.2:n.238-3769_238-3766del
NR_134982.2:n.238-3769_238-3766del