Canonical Allele Identifier: CA2569363
Gene: CD86 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1129055

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122119472G>A , CM000665.2:g.122119472G>A GRCh38
NC_000003.11:g.121838319G>A , CM000665.1:g.121838319G>A GRCh37
NC_000003.10:g.123321009G>A NCBI36
NG_029928.1:g.69111G>A

Transcript Alleles

HGVS Amino-acid change
NM_001206924.1:c.592G>A VV NP_001193853.1:p.Ala198Thr
NM_001206925.1:c.682G>A VV NP_001193854.1:p.Ala228Thr
NM_006889.4:c.910G>A VV NP_008820.3:p.Ala304Thr
NM_175862.4:c.928G>A VV NP_787058.4:p.Ala310Thr
NM_176892.1:c.766G>A VV NP_795711.1:p.Ala256Thr
ENST00000264468.9:c.766G>A ENSP00000264468.6:p.Ala256Thr
ENST00000330540.6:c.928G>A ENSP00000332049.2:p.Ala310Thr
ENST00000393627.6:c.910G>A ENSP00000377248.2:p.Ala304Thr
ENST00000469710.5:c.682G>A ENSP00000418988.1:p.Ala228Thr
ENST00000478741.1:n.770G>A
ENST00000493101.5:c.592G>A ENSP00000420230.1:p.Ala198Thr