Canonical Allele Identifier: CA942727249

Gene: CD3D

Linked Data

• dbSNP Id: rs1948286435
• gnomAD v3: 11-118340079-A-G
• gnomAD v4: 11-118340079-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118340079A>G , CM000673.2:g.118340079A>G	GRCh38
NC_000011.9:g.118210794A>G , CM000673.1:g.118210794A>G	GRCh37
NC_000011.8:g.117716004A>G	NCBI36
NG_007566.1:g.736A>G , LRG_39:g.736A>G
NG_009891.1:g.7666T>C , LRG_37:g.7666T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.589T>C
ENST00000695667.1:n.280-173T>C
ENST00000695668.1:n.2260-173T>C
ENST00000300692.9:c.275-173T>C MANE Select	ENSP00000300692.4:n.275-173T>C
ENST00000300692.8:c.275-173T>C	ENSP00000300692.4:n.275-173T>C
ENST00000392884.2:c.274+296T>C	ENSP00000376622.2:n.274+296T>C
ENST00000526561.1:n.80-585T>C
ENST00000529594.5:c.56-173T>C	ENSP00000437335.1:n.56-173T>C
ENST00000534687.5:c.287+296T>C
NM_000732.4:c.275-173T>C , LRG_37t1:c.275-173T>C	NP_000723.1:n.275-173T>C
NM_001040651.1:c.274+296T>C	NP_001035741.1:n.274+296T>C
NM_001040651.2:c.274+296T>C	NP_001035741.1:n.274+296T>C
NM_000732.6:c.275-173T>C MANE Select	NP_000723.1:n.275-173T>C