Canonical Allele Identifier: CA2003457097

Gene: CD3D

Linked Data

• dbSNP Id: rs1948285501
• gnomAD v4: 11-118339941-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339941A>G , CM000673.2:g.118339941A>G	GRCh38
NC_000011.9:g.118210656A>G , CM000673.1:g.118210656A>G	GRCh37
NC_000011.8:g.117715866A>G	NCBI36
NG_007566.1:g.598A>G , LRG_39:g.598A>G
NG_009891.1:g.7804T>C , LRG_37:g.7804T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695666.1:n.727T>C
ENST00000695667.1:n.280-35T>C
ENST00000695668.1:n.2260-35T>C
ENST00000300692.9:c.275-35T>C MANE Select	ENSP00000300692.4:n.275-35T>C
ENST00000300692.8:c.275-35T>C	ENSP00000300692.4:n.275-35T>C
ENST00000392884.2:c.274+434T>C	ENSP00000376622.2:n.274+434T>C
ENST00000526561.1:n.80-447T>C
ENST00000529594.5:c.56-35T>C	ENSP00000437335.1:n.56-35T>C
ENST00000534687.5:c.287+434T>C
NM_000732.4:c.275-35T>C , LRG_37t1:c.275-35T>C	NP_000723.1:n.275-35T>C
NM_001040651.1:c.274+434T>C	NP_001035741.1:n.274+434T>C
NM_001040651.2:c.274+434T>C	NP_001035741.1:n.274+434T>C
NM_000732.6:c.275-35T>C MANE Select	NP_000723.1:n.275-35T>C