Canonical Allele Identifier: CA10637733

Gene: CD3E

Linked Data

• ClinVar Variation Id: 302656
• ClinVar RCV Id: RCV000325470
• dbSNP Id: rs886047735
• gnomAD v2: 11-118175385-G-A
• gnomAD v3: 11-118304670-G-A
• gnomAD v4: 11-118304670-G-A
• MyVariant Identifiers: chr11:g.118175385G>A (hg19) ; chr11:g.118304670G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118304670G>A , CM000673.2:g.118304670G>A	GRCh38
NC_000011.9:g.118175385G>A , CM000673.1:g.118175385G>A	GRCh37
NC_000011.8:g.117680595G>A	NCBI36
NG_007383.1:g.5091G>A , LRG_38:g.5091G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361763.8:c.-166G>A	ENSP00000354566.4:n.-166G>A
NM_000733.3:c.-166G>A , LRG_38t1:c.-166G>A	NP_000724.1:n.-166G>A