Canonical Allele Identifier: CA354163975

Gene: CD86

Linked Data

• dbSNP Id: rs2107554337
• MyVariant Identifiers: chr3:g.121838378T>A (hg19) ; chr3:g.122119531T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119531T>A , CM000665.2:g.122119531T>A	GRCh38
NC_000003.11:g.121838378T>A , CM000665.1:g.121838378T>A	GRCh37
NC_000003.10:g.123321068T>A	NCBI36
NG_029928.1:g.69170T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.987T>A MANE Select	ENSP00000332049.2:p.Phe329Leu
ENST00000264468.9:c.825T>A	ENSP00000264468.6:p.Phe275Leu
ENST00000330540.6:c.987T>A	ENSP00000332049.2:p.Phe329Leu
ENST00000393627.6:c.969T>A	ENSP00000377248.2:p.Phe323Leu
ENST00000469710.5:c.741T>A	ENSP00000418988.1:p.Phe247Leu
ENST00000478741.1:c.829T>A
ENST00000493101.5:c.651T>A	ENSP00000420230.1:p.Phe217Leu
NM_001206924.1:c.651T>A	NP_001193853.1:p.Phe217Leu
NM_001206925.1:c.741T>A	NP_001193854.1:p.Phe247Leu
NM_006889.4:c.969T>A	NP_008820.3:p.Phe323Leu
NM_175862.4:c.987T>A	NP_787058.4:p.Phe329Leu
NM_176892.1:c.825T>A	NP_795711.1:p.Phe275Leu
NM_175862.5:c.987T>A MANE Select	NP_787058.5:p.Phe329Leu
NM_001206924.2:c.651T>A	NP_001193853.2:p.Phe217Leu
NM_001206925.2:c.741T>A	NP_001193854.2:p.Phe247Leu
NM_006889.5:c.969T>A	NP_008820.4:p.Phe323Leu
NM_176892.2:c.825T>A	NP_795711.2:p.Phe275Leu