Canonical Allele Identifier: CA354163859

Gene: CD86

Linked Data

• MyVariant Identifiers: chr3:g.121838328G>T (hg19) ; chr3:g.122119481G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119481G>T , CM000665.2:g.122119481G>T	GRCh38
NC_000003.11:g.121838328G>T , CM000665.1:g.121838328G>T	GRCh37
NC_000003.10:g.123321018G>T	NCBI36
NG_029928.1:g.69120G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.937G>T MANE Select	ENSP00000332049.2:p.Val313Phe
ENST00000264468.9:c.775G>T	ENSP00000264468.6:p.Val259Phe
ENST00000330540.6:c.937G>T	ENSP00000332049.2:p.Val313Phe
ENST00000393627.6:c.919G>T	ENSP00000377248.2:p.Val307Phe
ENST00000469710.5:c.691G>T	ENSP00000418988.1:p.Val231Phe
ENST00000478741.1:c.779G>T
ENST00000493101.5:c.601G>T	ENSP00000420230.1:p.Val201Phe
NM_001206924.1:c.601G>T	NP_001193853.1:p.Val201Phe
NM_001206925.1:c.691G>T	NP_001193854.1:p.Val231Phe
NM_006889.4:c.919G>T	NP_008820.3:p.Val307Phe
NM_175862.4:c.937G>T	NP_787058.4:p.Val313Phe
NM_176892.1:c.775G>T	NP_795711.1:p.Val259Phe
NM_175862.5:c.937G>T MANE Select	NP_787058.5:p.Val313Phe
NM_001206924.2:c.601G>T	NP_001193853.2:p.Val201Phe
NM_001206925.2:c.691G>T	NP_001193854.2:p.Val231Phe
NM_006889.5:c.919G>T	NP_008820.4:p.Val307Phe
NM_176892.2:c.775G>T	NP_795711.2:p.Val259Phe