Canonical Allele Identifier: CA229501120
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs201879931
gnomAD v2: 11-118183322-T-C
MyVariant Identifiers: chr11:g.118183322T>C (hg19) chr11:g.118312607T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312607T>C , CM000673.2:g.118312607T>C GRCh38
NC_000011.9:g.118183322T>C , CM000673.1:g.118183322T>C GRCh37
NC_000011.8:g.117688532T>C NCBI36
NG_007383.1:g.13028T>C , LRG_38:g.13028T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361763.9:c.104-11T>C MANE Select ENSP00000354566.4:n.104-11T>C
ENST00000361763.8:c.104-11T>C ENSP00000354566.4:n.104-11T>C
ENST00000526146.5:n.639T>C
ENST00000528435.5:n.646T>C
ENST00000528600.1:c.86-11T>C ENSP00000433975.1:n.86-11T>C
ENST00000529713.5:n.210-11T>C
ENST00000531913.1:n.464T>C
NM_000733.3:c.104-11T>C , LRG_38t1:c.104-11T>C NP_000724.1:n.104-11T>C
NM_000733.4:c.104-11T>C MANE Select NP_000724.1:n.104-11T>C
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