Canonical Allele Identifier: CA354163866

Gene: CD86

Linked Data

• MyVariant Identifiers: chr3:g.121838331T>G (hg19) ; chr3:g.122119484T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119484T>G , CM000665.2:g.122119484T>G	GRCh38
NC_000003.11:g.121838331T>G , CM000665.1:g.121838331T>G	GRCh37
NC_000003.10:g.123321021T>G	NCBI36
NG_029928.1:g.69123T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.940T>G MANE Select	ENSP00000332049.2:p.Phe314Val
ENST00000264468.9:c.778T>G	ENSP00000264468.6:p.Phe260Val
ENST00000330540.6:c.940T>G	ENSP00000332049.2:p.Phe314Val
ENST00000393627.6:c.922T>G	ENSP00000377248.2:p.Phe308Val
ENST00000469710.5:c.694T>G	ENSP00000418988.1:p.Phe232Val
ENST00000478741.1:c.782T>G
ENST00000493101.5:c.604T>G	ENSP00000420230.1:p.Phe202Val
NM_001206924.1:c.604T>G	NP_001193853.1:p.Phe202Val
NM_001206925.1:c.694T>G	NP_001193854.1:p.Phe232Val
NM_006889.4:c.922T>G	NP_008820.3:p.Phe308Val
NM_175862.4:c.940T>G	NP_787058.4:p.Phe314Val
NM_176892.1:c.778T>G	NP_795711.1:p.Phe260Val
NM_175862.5:c.940T>G MANE Select	NP_787058.5:p.Phe314Val
NM_001206924.2:c.604T>G	NP_001193853.2:p.Phe202Val
NM_001206925.2:c.694T>G	NP_001193854.2:p.Phe232Val
NM_006889.5:c.922T>G	NP_008820.4:p.Phe308Val
NM_176892.2:c.778T>G	NP_795711.2:p.Phe260Val