Canonical Allele Identifier: CA435252272

Gene: CD86

Linked Data

• gnomAD v4: 3-122119477-G-A
• MyVariant Identifiers: chr3:g.121838324G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119477G>A , CM000665.2:g.122119477G>A	GRCh38
NC_000003.11:g.121838324G>A , CM000665.1:g.121838324G>A	GRCh37
NC_000003.10:g.123321014G>A	NCBI36
NG_029928.1:g.69116G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.933G>A MANE Select	ENSP00000332049.2:p.Gln311=
ENST00000264468.9:c.771G>A	ENSP00000264468.6:p.Gln257=
ENST00000330540.6:c.933G>A	ENSP00000332049.2:p.Gln311=
ENST00000393627.6:c.915G>A	ENSP00000377248.2:p.Gln305=
ENST00000469710.5:c.687G>A	ENSP00000418988.1:p.Gln229=
ENST00000478741.1:c.775G>A
ENST00000493101.5:c.597G>A	ENSP00000420230.1:p.Gln199=
NM_001206924.1:c.597G>A	NP_001193853.1:p.Gln199=
NM_001206925.1:c.687G>A	NP_001193854.1:p.Gln229=
NM_006889.4:c.915G>A	NP_008820.3:p.Gln305=
NM_175862.4:c.933G>A	NP_787058.4:p.Gln311=
NM_176892.1:c.771G>A	NP_795711.1:p.Gln257=
NM_175862.5:c.933G>A MANE Select	NP_787058.5:p.Gln311=
NM_001206924.2:c.597G>A	NP_001193853.2:p.Gln199=
NM_001206925.2:c.687G>A	NP_001193854.2:p.Gln229=
NM_006889.5:c.915G>A	NP_008820.4:p.Gln305=
NM_176892.2:c.771G>A	NP_795711.2:p.Gln257=