Canonical Allele Identifier: CA22904931

Gene: CYP2J2

Linked Data

• dbSNP Id: rs766671773
• gnomAD v2: 1-60385661-AGACT-A
• gnomAD v3: 1-59919989-AGACT-A
• gnomAD v4: 1-59919989-AGACT-A
• MyVariant Identifiers: chr1:g.60385662_60385665del (hg19) ; chr1:g.59919990_59919993del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59919995_59919998del , CM000663.2:g.59919995_59919998del	GRCh38
NC_000001.10:g.60385667_60385670del , CM000663.1:g.60385667_60385670del	GRCh37
NC_000001.9:g.60158255_60158258del	NCBI36
NG_007931.1:g.11759_11762del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-3893_211-3890del MANE Select	ENSP00000360247.3:n.211-3893_211-3890del
ENST00000468257.2:c.211-3893_211-3890del	ENSP00000497807.1:n.211-3893_211-3890del
ENST00000469406.6:c.227-3893_227-3890del	ENSP00000497732.1:n.227-3893_227-3890del
ENST00000371204.3:c.211-3893_211-3890del	ENSP00000360247.3:n.211-3893_211-3890del
ENST00000466095.5:n.226-3893_226-3890del
ENST00000468257.1:n.236-3893_236-3890del
ENST00000469406.5:n.226-3893_226-3890del
NM_000775.2:c.211-3893_211-3890del	NP_000766.2:n.211-3893_211-3890del
XR_246240.2:n.238-3893_238-3890del
XR_946558.1:n.238-3893_238-3890del
NM_000775.3:c.211-3893_211-3890del	NP_000766.2:n.211-3893_211-3890del
NR_134981.1:n.263-3893_263-3890del
NR_134982.1:n.263-3893_263-3890del
NM_000775.4:c.211-3893_211-3890del MANE Select	NP_000766.2:n.211-3893_211-3890del
NR_134981.2:n.238-3893_238-3890del
NR_134982.2:n.238-3893_238-3890del