Canonical Allele Identifier: CA2696033639
Gene: CYP2J2 HGNC NCBI

Linked Data

dbSNP Id: rs2102135883

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59920064del , CM000663.2:g.59920064del GRCh38
NC_000001.10:g.60385736del , CM000663.1:g.60385736del GRCh37
NC_000001.9:g.60158324del NCBI36
NG_007931.1:g.11690del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371204.4:c.211-3962del MANE Select ENSP00000360247.3:n.211-3962del
ENST00000468257.2:c.211-3962del ENSP00000497807.1:n.211-3962del
ENST00000469406.6:c.227-3962del ENSP00000497732.1:n.227-3962del
ENST00000371204.3:c.211-3962del ENSP00000360247.3:n.211-3962del
ENST00000466095.5:n.226-3962del
ENST00000468257.1:n.236-3962del
ENST00000469406.5:n.226-3962del
NM_000775.2:c.211-3962del NP_000766.2:n.211-3962del
XR_246240.2:n.238-3962del
XR_946558.1:n.238-3962del
NM_000775.3:c.211-3962del NP_000766.2:n.211-3962del
NR_134981.1:n.263-3962del
NR_134982.1:n.263-3962del
NM_000775.4:c.211-3962del MANE Select NP_000766.2:n.211-3962del
NR_134981.2:n.238-3962del
NR_134982.2:n.238-3962del