Canonical Allele Identifier: CA672356355

Gene: CD3D

Linked Data

• dbSNP Id: rs1333716335
• gnomAD v3: 11-118339723-C-G
• gnomAD v4: 11-118339723-C-G
• MyVariant Identifiers: chr11:g.118210438C>G (hg19) ; chr11:g.118339723C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339723C>G , CM000673.2:g.118339723C>G	GRCh38
NC_000011.9:g.118210438C>G , CM000673.1:g.118210438C>G	GRCh37
NC_000011.8:g.117715648C>G	NCBI36
NG_007566.1:g.380C>G , LRG_39:g.380C>G
NG_009891.1:g.8022G>C , LRG_37:g.8022G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.945G>C
ENST00000695667.1:n.463G>C
ENST00000695668.1:n.2443G>C
ENST00000300692.9:c.406+52G>C MANE Select	ENSP00000300692.4:n.406+52G>C
ENST00000300692.8:c.406+52G>C	ENSP00000300692.4:n.406+52G>C
ENST00000392884.2:c.275-229G>C	ENSP00000376622.2:n.275-229G>C
ENST00000526561.1:n.80-229G>C
ENST00000529594.5:c.187+52G>C	ENSP00000437335.1:n.187+52G>C
ENST00000534687.5:c.288-229G>C
NM_000732.4:c.406+52G>C , LRG_37t1:c.406+52G>C	NP_000723.1:n.406+52G>C
NM_001040651.1:c.275-229G>C	NP_001035741.1:n.275-229G>C
NM_001040651.2:c.275-229G>C	NP_001035741.1:n.275-229G>C
NM_000732.6:c.406+52G>C MANE Select	NP_000723.1:n.406+52G>C