Canonical Allele Identifier: CA1002240166

Gene: CYP2J2

Linked Data

• dbSNP Id: rs1644530571
• gnomAD v3: 1-59922926-T-C
• gnomAD v4: 1-59922926-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59922926T>C , CM000663.2:g.59922926T>C	GRCh38
NC_000001.10:g.60388598T>C , CM000663.1:g.60388598T>C	GRCh37
NC_000001.9:g.60161186T>C	NCBI36
NG_007931.1:g.8826A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371204.4:c.210+3611A>G MANE Select	ENSP00000360247.3:n.210+3611A>G
ENST00000468257.2:c.210+3611A>G	ENSP00000497807.1:n.210+3611A>G
ENST00000469406.6:c.226+3595A>G	ENSP00000497732.1:n.226+3595A>G
ENST00000371204.3:c.210+3611A>G	ENSP00000360247.3:n.210+3611A>G
ENST00000466095.5:n.225+3611A>G
ENST00000468257.1:n.235+3595A>G
ENST00000469406.5:n.225+3611A>G
NM_000775.2:c.210+3611A>G	NP_000766.2:n.210+3611A>G
XR_246240.2:n.237+3611A>G
XR_946558.1:n.237+3611A>G
NM_000775.3:c.210+3611A>G	NP_000766.2:n.210+3611A>G
NR_134981.1:n.262+3611A>G
NR_134982.1:n.262+3611A>G
NM_000775.4:c.210+3611A>G MANE Select	NP_000766.2:n.210+3611A>G
NR_134981.2:n.237+3611A>G
NR_134982.2:n.237+3611A>G