Canonical Allele Identifier: CA382792287

Gene: CD3G

Linked Data

• MyVariant Identifiers: chr11:g.118220489A>C (hg19) ; chr11:g.118349774A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118349774A>C , CM000673.2:g.118349774A>C	GRCh38
NC_000011.9:g.118220489A>C , CM000673.1:g.118220489A>C	GRCh37
NC_000011.8:g.117725699A>C	NCBI36
NG_007566.1:g.10431A>C , LRG_39:g.10431A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000532917.3:c.111A>C MANE Select	ENSP00000431445.2:p.Gln37His
ENST00000292144.8:c.*168A>C	ENSP00000292144.4:n.*168A>C
ENST00000392883.6:c.-70A>C	ENSP00000376621.2:n.-70A>C
ENST00000527777.5:n.191A>C
ENST00000528540.5:n.132A>C
ENST00000532903.1:n.187A>C
ENST00000532917.1:c.111A>C	ENSP00000431445.1:p.Gln37His
ENST00000533462.5:n.883A>C
NM_000073.2:c.111A>C , LRG_39t1:c.111A>C	NP_000064.1:p.Gln37His
XM_005271724.2:c.111A>C	XP_005271781.1:p.Gln37His
XM_006718941.2:c.111A>C	XP_006719004.1:p.Gln37His
XM_005271724.4:c.111A>C	XP_005271781.1:p.Gln37His
XM_006718941.3:c.111A>C	XP_006719004.1:p.Gln37His
NM_000073.3:c.111A>C MANE Select	NP_000064.1:p.Gln37His