Canonical Allele Identifier: CA229495506
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs531169032
gnomAD v2: 11-118175271-T-C
gnomAD v3: 11-118304556-T-C
gnomAD v4: 11-118304556-T-C
MyVariant Identifiers: chr11:g.118175271T>C (hg19) chr11:g.118304556T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118304556T>C , CM000673.2:g.118304556T>C GRCh38
NC_000011.9:g.118175271T>C , CM000673.1:g.118175271T>C GRCh37
NC_000011.8:g.117680481T>C NCBI36
NG_007383.1:g.4977T>C , LRG_38:g.4977T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.8:c.-280T>C ENSP00000354566.4:n.-280T>C
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