Canonical Allele Identifier: CA477356309

Gene: CD3G

Linked Data

• gnomAD v4: 11-118349771-T-C
• MyVariant Identifiers: chr11:g.118220486T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118349771T>C , CM000673.2:g.118349771T>C	GRCh38
NC_000011.9:g.118220486T>C , CM000673.1:g.118220486T>C	GRCh37
NC_000011.8:g.117725696T>C	NCBI36
NG_007566.1:g.10428T>C , LRG_39:g.10428T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000532917.3:c.108T>C MANE Select	ENSP00000431445.2:p.Tyr36=
ENST00000292144.8:c.*165T>C	ENSP00000292144.4:n.*165T>C
ENST00000392883.6:c.-73T>C	ENSP00000376621.2:n.-73T>C
ENST00000527777.5:n.188T>C
ENST00000528540.5:n.129T>C
ENST00000532903.1:n.184T>C
ENST00000532917.1:c.108T>C	ENSP00000431445.1:p.Tyr36=
ENST00000533462.5:n.880T>C
NM_000073.2:c.108T>C , LRG_39t1:c.108T>C	NP_000064.1:p.Tyr36=
XM_005271724.2:c.108T>C	XP_005271781.1:p.Tyr36=
XM_006718941.2:c.108T>C	XP_006719004.1:p.Tyr36=
XM_005271724.4:c.108T>C	XP_005271781.1:p.Tyr36=
XM_006718941.3:c.108T>C	XP_006719004.1:p.Tyr36=
NM_000073.3:c.108T>C MANE Select	NP_000064.1:p.Tyr36=