Canonical Allele Identifier: CA942727314

Gene: CD3D

Linked Data

• dbSNP Id: rs1948287152
• gnomAD v3: 11-118340224-T-C
• gnomAD v4: 11-118340224-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118340224T>C , CM000673.2:g.118340224T>C	GRCh38
NC_000011.9:g.118210939T>C , CM000673.1:g.118210939T>C	GRCh37
NC_000011.8:g.117716149T>C	NCBI36
NG_007566.1:g.881T>C , LRG_39:g.881T>C
NG_009891.1:g.7521A>G , LRG_37:g.7521A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.444A>G
ENST00000695667.1:n.279+151A>G
ENST00000695668.1:n.2259+151A>G
ENST00000300692.9:c.274+151A>G MANE Select	ENSP00000300692.4:n.274+151A>G
ENST00000300692.8:c.274+151A>G	ENSP00000300692.4:n.274+151A>G
ENST00000392884.2:c.274+151A>G	ENSP00000376622.2:n.274+151A>G
ENST00000526561.1:n.80-730A>G
ENST00000529594.5:c.56-318A>G	ENSP00000437335.1:n.56-318A>G
ENST00000534687.5:c.287+151A>G
NM_000732.4:c.274+151A>G , LRG_37t1:c.274+151A>G	NP_000723.1:n.274+151A>G
NM_001040651.1:c.274+151A>G	NP_001035741.1:n.274+151A>G
NM_001040651.2:c.274+151A>G	NP_001035741.1:n.274+151A>G
NM_000732.6:c.274+151A>G MANE Select	NP_000723.1:n.274+151A>G