Canonical Allele Identifier: CA477081933
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs1948141777
MyVariant Identifiers: chr11:g.118183334A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312619A>G , CM000673.2:g.118312619A>G GRCh38
NC_000011.9:g.118183334A>G , CM000673.1:g.118183334A>G GRCh37
NC_000011.8:g.117688544A>G NCBI36
NG_007383.1:g.13040A>G , LRG_38:g.13040A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361763.9:c.105A>G MANE Select ENSP00000354566.4:p.Pro35=
ENST00000361763.8:c.105A>G ENSP00000354566.4:p.Pro35=
ENST00000526146.5:n.651A>G
ENST00000528435.5:n.658A>G
ENST00000528600.1:c.87A>G ENSP00000433975.1:p.Ala29=
ENST00000529713.5:n.211A>G
ENST00000531913.1:n.476A>G
NM_000733.3:c.105A>G , LRG_38t1:c.105A>G NP_000724.1:p.Pro35=
NM_000733.4:c.105A>G MANE Select NP_000724.1:p.Pro35=