Canonical Allele Identifier: CA737469293

Gene: CYP2J2

Linked Data

• dbSNP Id: rs1250703026
• gnomAD v3: 1-59919907-G-A
• gnomAD v4: 1-59919907-G-A
• MyVariant Identifiers: chr1:g.60385579G>A (hg19) ; chr1:g.59919907G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59919907G>A , CM000663.2:g.59919907G>A	GRCh38
NC_000001.10:g.60385579G>A , CM000663.1:g.60385579G>A	GRCh37
NC_000001.9:g.60158167G>A	NCBI36
NG_007931.1:g.11845C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-3807C>T MANE Select	ENSP00000360247.3:n.211-3807C>T
ENST00000468257.2:c.211-3807C>T	ENSP00000497807.1:n.211-3807C>T
ENST00000469406.6:c.227-3807C>T	ENSP00000497732.1:n.227-3807C>T
ENST00000371204.3:c.211-3807C>T	ENSP00000360247.3:n.211-3807C>T
ENST00000466095.5:n.226-3807C>T
ENST00000468257.1:n.236-3807C>T
ENST00000469406.5:n.226-3807C>T
NM_000775.2:c.211-3807C>T	NP_000766.2:n.211-3807C>T
XR_246240.2:n.238-3807C>T
XR_946558.1:n.238-3807C>T
NM_000775.3:c.211-3807C>T	NP_000766.2:n.211-3807C>T
NR_134981.1:n.263-3807C>T
NR_134982.1:n.263-3807C>T
NM_000775.4:c.211-3807C>T MANE Select	NP_000766.2:n.211-3807C>T
NR_134981.2:n.238-3807C>T
NR_134982.2:n.238-3807C>T