Canonical Allele Identifier: CA1170018030
Gene: CYP2J2 HGNC NCBI

Linked Data

dbSNP Id: rs1155002

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59908103T>G , CM000663.2:g.59908103T>G GRCh38
NC_000001.10:g.60373775T>G , CM000663.1:g.60373775T>G GRCh37
NC_000001.9:g.60146363T>G NCBI36
NG_007931.1:g.23649A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371204.4:c.862-176A>C MANE Select ENSP00000360247.3:n.862-176A>C
ENST00000468257.2:c.862-176A>C ENSP00000497807.1:n.862-176A>C
ENST00000469406.6:c.*623-176A>C ENSP00000497732.1:n.*623-176A>C
ENST00000371204.3:c.862-176A>C ENSP00000360247.3:n.862-176A>C
ENST00000466095.5:n.877-176A>C
ENST00000469406.5:n.877-176A>C
ENST00000492633.5:n.1416-176A>C
NM_000775.2:c.862-176A>C NP_000766.2:n.862-176A>C
XR_246240.2:n.889-176A>C
XR_946558.1:n.889-176A>C
NM_000775.3:c.862-176A>C NP_000766.2:n.862-176A>C
NR_134981.1:n.914-176A>C
NR_134982.1:n.914-176A>C
NM_000775.4:c.862-176A>C MANE Select NP_000766.2:n.862-176A>C
NR_134981.2:n.889-176A>C
NR_134982.2:n.889-176A>C