Canonical Allele Identifier: CA2569367

Gene: CD86

Linked Data

• ClinVar Variation Id: 2392164
• ClinVar RCV Id: RCV002733572
• dbSNP Id: rs370380261
• ExAC: 3:121838326 G / A
• gnomAD v2: 3-121838326-G-A
• gnomAD v3: 3-122119479-G-A
• gnomAD v4: 3-122119479-G-A
• COSMIC: COSM1418237
• MyVariant Identifiers: chr3:g.121838326G>A (hg19) ; chr3:g.122119479G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119479G>A , CM000665.2:g.122119479G>A	GRCh38
NC_000003.11:g.121838326G>A , CM000665.1:g.121838326G>A	GRCh37
NC_000003.10:g.123321016G>A	NCBI36
NG_029928.1:g.69118G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.935G>A MANE Select	ENSP00000332049.2:p.Arg312His
ENST00000264468.9:c.773G>A	ENSP00000264468.6:p.Arg258His
ENST00000330540.6:c.935G>A	ENSP00000332049.2:p.Arg312His
ENST00000393627.6:c.917G>A	ENSP00000377248.2:p.Arg306His
ENST00000469710.5:c.689G>A	ENSP00000418988.1:p.Arg230His
ENST00000478741.1:c.777G>A
ENST00000493101.5:c.599G>A	ENSP00000420230.1:p.Arg200His
NM_001206924.1:c.599G>A	NP_001193853.1:p.Arg200His
NM_001206925.1:c.689G>A	NP_001193854.1:p.Arg230His
NM_006889.4:c.917G>A	NP_008820.3:p.Arg306His
NM_175862.4:c.935G>A	NP_787058.4:p.Arg312His
NM_176892.1:c.773G>A	NP_795711.1:p.Arg258His
NM_175862.5:c.935G>A MANE Select	NP_787058.5:p.Arg312His
NM_001206924.2:c.599G>A	NP_001193853.2:p.Arg200His
NM_001206925.2:c.689G>A	NP_001193854.2:p.Arg230His
NM_006889.5:c.917G>A	NP_008820.4:p.Arg306His
NM_176892.2:c.773G>A	NP_795711.2:p.Arg258His