Canonical Allele Identifier: CA898096202

Gene: CD86

Linked Data

• dbSNP Id: rs1015774591
• gnomAD v3: 3-122066794-C-T
• gnomAD v4: 3-122066794-C-T
• MyVariant Identifiers: chr3:g.121785641C>T (hg19) ; chr3:g.122066794C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122066794C>T , CM000665.2:g.122066794C>T	GRCh38
NC_000003.11:g.121785641C>T , CM000665.1:g.121785641C>T	GRCh37
NC_000003.10:g.123268331C>T	NCBI36
NG_029928.1:g.16433C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.14+11291C>T MANE Select	ENSP00000332049.2:n.14+11291C>T
ENST00000330540.6:c.14+11291C>T	ENSP00000332049.2:n.14+11291C>T
ENST00000469710.5:c.-183+11291C>T	ENSP00000418988.1:n.-183+11291C>T
ENST00000478390.1:n.127+11291C>T
ENST00000493101.5:c.14+11291C>T	ENSP00000420230.1:n.14+11291C>T
NM_001206924.1:c.14+11291C>T	NP_001193853.1:n.14+11291C>T
NM_001206925.1:c.-183+11291C>T	NP_001193854.1:n.-183+11291C>T
NM_175862.4:c.14+11291C>T	NP_787058.4:n.14+11291C>T
NM_175862.5:c.14+11291C>T MANE Select	NP_787058.5:n.14+11291C>T
NM_001206924.2:c.14+11291C>T	NP_001193853.2:n.14+11291C>T
NM_001206925.2:c.-183+11291C>T	NP_001193854.2:n.-183+11291C>T