Canonical Allele Identifier: CA22904900

Gene: CYP2J2

Linked Data

• dbSNP Id: rs910592937
• gnomAD v2: 1-60385577-C-T
• gnomAD v3: 1-59919905-C-T
• gnomAD v4: 1-59919905-C-T
• MyVariant Identifiers: chr1:g.60385577C>T (hg19) ; chr1:g.59919905C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59919905C>T , CM000663.2:g.59919905C>T	GRCh38
NC_000001.10:g.60385577C>T , CM000663.1:g.60385577C>T	GRCh37
NC_000001.9:g.60158165C>T	NCBI36
NG_007931.1:g.11847G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-3805G>A MANE Select	ENSP00000360247.3:n.211-3805G>A
ENST00000468257.2:c.211-3805G>A	ENSP00000497807.1:n.211-3805G>A
ENST00000469406.6:c.227-3805G>A	ENSP00000497732.1:n.227-3805G>A
ENST00000371204.3:c.211-3805G>A	ENSP00000360247.3:n.211-3805G>A
ENST00000466095.5:n.226-3805G>A
ENST00000468257.1:n.236-3805G>A
ENST00000469406.5:n.226-3805G>A
NM_000775.2:c.211-3805G>A	NP_000766.2:n.211-3805G>A
XR_246240.2:n.238-3805G>A
XR_946558.1:n.238-3805G>A
NM_000775.3:c.211-3805G>A	NP_000766.2:n.211-3805G>A
NR_134981.1:n.263-3805G>A
NR_134982.1:n.263-3805G>A
NM_000775.4:c.211-3805G>A MANE Select	NP_000766.2:n.211-3805G>A
NR_134981.2:n.238-3805G>A
NR_134982.2:n.238-3805G>A