Canonical Allele Identifier: CA435252286

Gene: CD86

Linked Data

• MyVariant Identifiers: chr3:g.121838348A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119501A>T , CM000665.2:g.122119501A>T	GRCh38
NC_000003.11:g.121838348A>T , CM000665.1:g.121838348A>T	GRCh37
NC_000003.10:g.123321038A>T	NCBI36
NG_029928.1:g.69140A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.957A>T MANE Select	ENSP00000332049.2:p.Thr319=
ENST00000264468.9:c.795A>T	ENSP00000264468.6:p.Thr265=
ENST00000330540.6:c.957A>T	ENSP00000332049.2:p.Thr319=
ENST00000393627.6:c.939A>T	ENSP00000377248.2:p.Thr313=
ENST00000469710.5:c.711A>T	ENSP00000418988.1:p.Thr237=
ENST00000478741.1:c.799A>T
ENST00000493101.5:c.621A>T	ENSP00000420230.1:p.Thr207=
NM_001206924.1:c.621A>T	NP_001193853.1:p.Thr207=
NM_001206925.1:c.711A>T	NP_001193854.1:p.Thr237=
NM_006889.4:c.939A>T	NP_008820.3:p.Thr313=
NM_175862.4:c.957A>T	NP_787058.4:p.Thr319=
NM_176892.1:c.795A>T	NP_795711.1:p.Thr265=
NM_175862.5:c.957A>T MANE Select	NP_787058.5:p.Thr319=
NM_001206924.2:c.621A>T	NP_001193853.2:p.Thr207=
NM_001206925.2:c.711A>T	NP_001193854.2:p.Thr237=
NM_006889.5:c.939A>T	NP_008820.4:p.Thr313=
NM_176892.2:c.795A>T	NP_795711.2:p.Thr265=