Canonical Allele Identifier: CA22904949

Gene: CYP2J2

Linked Data

• dbSNP Id: rs11572224
• gnomAD v2: 1-60385703-CAT-C
• gnomAD v3: 1-59920031-CAT-C
• gnomAD v4: 1-59920031-CAT-C
• MyVariant Identifiers: chr1:g.60385704_60385705del (hg19) ; chr1:g.59920032_59920033del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59920032_59920033del , CM000663.2:g.59920032_59920033del	GRCh38
NC_000001.10:g.60385704_60385705del , CM000663.1:g.60385704_60385705del	GRCh37
NC_000001.9:g.60158292_60158293del	NCBI36
NG_007931.1:g.11719_11720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371204.4:c.211-3933_211-3932del MANE Select	ENSP00000360247.3:n.211-3933_211-3932del
ENST00000468257.2:c.211-3933_211-3932del	ENSP00000497807.1:n.211-3933_211-3932del
ENST00000469406.6:c.227-3933_227-3932del	ENSP00000497732.1:n.227-3933_227-3932del
ENST00000371204.3:c.211-3933_211-3932del	ENSP00000360247.3:n.211-3933_211-3932del
ENST00000466095.5:n.226-3933_226-3932del
ENST00000468257.1:n.236-3933_236-3932del
ENST00000469406.5:n.226-3933_226-3932del
NM_000775.2:c.211-3933_211-3932del	NP_000766.2:n.211-3933_211-3932del
XR_246240.2:n.238-3933_238-3932del
XR_946558.1:n.238-3933_238-3932del
NM_000775.3:c.211-3933_211-3932del	NP_000766.2:n.211-3933_211-3932del
NR_134981.1:n.263-3933_263-3932del
NR_134982.1:n.263-3933_263-3932del
NM_000775.4:c.211-3933_211-3932del MANE Select	NP_000766.2:n.211-3933_211-3932del
NR_134981.2:n.238-3933_238-3932del
NR_134982.2:n.238-3933_238-3932del