Canonical Allele Identifier: CA2569365

Gene: CD86

Linked Data

• ClinVar Variation Id: 3140701
• ClinVar RCV Id: RCV004435573
• dbSNP Id: rs201148004
• ExAC: 3:121838325 C / T
• gnomAD v2: 3-121838325-C-T
• gnomAD v3: 3-122119478-C-T
• gnomAD v4: 3-122119478-C-T
• MyVariant Identifiers: chr3:g.121838325C>T (hg19) ; chr3:g.122119478C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119478C>T , CM000665.2:g.122119478C>T	GRCh38
NC_000003.11:g.121838325C>T , CM000665.1:g.121838325C>T	GRCh37
NC_000003.10:g.123321015C>T	NCBI36
NG_029928.1:g.69117C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.934C>T MANE Select	ENSP00000332049.2:p.Arg312Cys
ENST00000264468.9:c.772C>T	ENSP00000264468.6:p.Arg258Cys
ENST00000330540.6:c.934C>T	ENSP00000332049.2:p.Arg312Cys
ENST00000393627.6:c.916C>T	ENSP00000377248.2:p.Arg306Cys
ENST00000469710.5:c.688C>T	ENSP00000418988.1:p.Arg230Cys
ENST00000478741.1:c.776C>T
ENST00000493101.5:c.598C>T	ENSP00000420230.1:p.Arg200Cys
NM_001206924.1:c.598C>T	NP_001193853.1:p.Arg200Cys
NM_001206925.1:c.688C>T	NP_001193854.1:p.Arg230Cys
NM_006889.4:c.916C>T	NP_008820.3:p.Arg306Cys
NM_175862.4:c.934C>T	NP_787058.4:p.Arg312Cys
NM_176892.1:c.772C>T	NP_795711.1:p.Arg258Cys
NM_175862.5:c.934C>T MANE Select	NP_787058.5:p.Arg312Cys
NM_001206924.2:c.598C>T	NP_001193853.2:p.Arg200Cys
NM_001206925.2:c.688C>T	NP_001193854.2:p.Arg230Cys
NM_006889.5:c.916C>T	NP_008820.4:p.Arg306Cys
NM_176892.2:c.772C>T	NP_795711.2:p.Arg258Cys