Canonical Allele Identifier: CA229495586
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs558912571
gnomAD v2: 11-118175407-G-A
gnomAD v3: 11-118304692-G-A
gnomAD v4: 11-118304692-G-A
MyVariant Identifiers: chr11:g.118175407G>A (hg19) chr11:g.118304692G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118304692G>A , CM000673.2:g.118304692G>A GRCh38
NC_000011.9:g.118175407G>A , CM000673.1:g.118175407G>A GRCh37
NC_000011.8:g.117680617G>A NCBI36
NG_007383.1:g.5113G>A , LRG_38:g.5113G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361763.8:c.-144G>A ENSP00000354566.4:n.-144G>A
NM_000733.3:c.-144G>A , LRG_38t1:c.-144G>A NP_000724.1:n.-144G>A
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