Canonical Allele Identifier: CA11600563
Gene: CD86 HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.122077921G>A
GRCh37 chr3:g.121796768G>A
gnomAD v2:
3:121796768 G / A
gnomAD v3:
3:122077921 G / A
gnomAD v4:
chr3-122077921-G-A
Joint Max Group AF 0.10216797 (SAS)
Genomes Max Group AF 0.08854526 (SAS)
Exomes Max Group AF 0.10455475 (SAS)
dbSNP:
9282641
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122077921G>A , CM000665.2:g.122077921G>A GRCh38
NC_000003.11:g.121796768G>A , CM000665.1:g.121796768G>A GRCh37
NC_000003.10:g.123279458G>A NCBI36
NG_029928.1:g.27560G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330540.7:c.15-13680G>A MANE Select ENSP00000332049.2:n.15-13680G>A
ENST00000264468.9:c.-129G>A ENSP00000264468.6:n.-129G>A
ENST00000330540.6:c.15-13680G>A ENSP00000332049.2:n.15-13680G>A
ENST00000393627.6:c.-129G>A ENSP00000377248.2:n.-129G>A
ENST00000469710.5:c.-183+22418G>A ENSP00000418988.1:n.-183+22418G>A
ENST00000478390.1:n.128-13680G>A
ENST00000482356.5:c.-5+5G>A ENSP00000419116.1:n.-5+5G>A
ENST00000483949.1:n.78G>A
ENST00000493101.5:c.15-13680G>A ENSP00000420230.1:n.15-13680G>A
NM_001206924.1:c.15-13680G>A NP_001193853.1:n.15-13680G>A
NM_001206925.1:c.-183+22418G>A NP_001193854.1:n.-183+22418G>A
NM_006889.4:c.-129G>A NP_008820.3:n.-129G>A
NM_175862.4:c.15-13680G>A NP_787058.4:n.15-13680G>A
NM_176892.1:c.-129G>A NP_795711.1:n.-129G>A
NM_175862.5:c.15-13680G>A MANE Select NP_787058.5:n.15-13680G>A
NM_001206924.2:c.15-13680G>A NP_001193853.2:n.15-13680G>A
NM_001206925.2:c.-183+22418G>A NP_001193854.2:n.-183+22418G>A
NM_006889.5:c.-129G>A NP_008820.4:n.-129G>A
NM_176892.2:c.-129G>A NP_795711.2:n.-129G>A
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