Canonical Allele Identifier: CA22904989

Gene: CYP2J2

Linked Data

• dbSNP Id: rs747322014
• gnomAD v2: 1-60385773-T-C
• gnomAD v3: 1-59920101-T-C
• gnomAD v4: 1-59920101-T-C
• MyVariant Identifiers: chr1:g.60385773T>C (hg19) ; chr1:g.59920101T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59920101T>C , CM000663.2:g.59920101T>C	GRCh38
NC_000001.10:g.60385773T>C , CM000663.1:g.60385773T>C	GRCh37
NC_000001.9:g.60158361T>C	NCBI36
NG_007931.1:g.11651A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-4001A>G MANE Select	ENSP00000360247.3:n.211-4001A>G
ENST00000468257.2:c.211-4001A>G	ENSP00000497807.1:n.211-4001A>G
ENST00000469406.6:c.227-4001A>G	ENSP00000497732.1:n.227-4001A>G
ENST00000371204.3:c.211-4001A>G	ENSP00000360247.3:n.211-4001A>G
ENST00000466095.5:n.226-4001A>G
ENST00000468257.1:n.236-4001A>G
ENST00000469406.5:n.226-4001A>G
NM_000775.2:c.211-4001A>G	NP_000766.2:n.211-4001A>G
XR_246240.2:n.238-4001A>G
XR_946558.1:n.238-4001A>G
NM_000775.3:c.211-4001A>G	NP_000766.2:n.211-4001A>G
NR_134981.1:n.263-4001A>G
NR_134982.1:n.263-4001A>G
NM_000775.4:c.211-4001A>G MANE Select	NP_000766.2:n.211-4001A>G
NR_134981.2:n.238-4001A>G
NR_134982.2:n.238-4001A>G