Canonical Allele Identifier: CA82750697

Gene: CD86

Linked Data

• dbSNP Id: rs913993332
• gnomAD v4: 3-122119452-T-C
• MyVariant Identifiers: chr3:g.121838299T>C (hg19) ; chr3:g.122119452T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119452T>C , CM000665.2:g.122119452T>C	GRCh38
NC_000003.11:g.121838299T>C , CM000665.1:g.121838299T>C	GRCh37
NC_000003.10:g.123320989T>C	NCBI36
NG_029928.1:g.69091T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.908T>C MANE Select	ENSP00000332049.2:p.Ile303Thr
ENST00000264468.9:c.746T>C	ENSP00000264468.6:p.Ile249Thr
ENST00000330540.6:c.908T>C	ENSP00000332049.2:p.Ile303Thr
ENST00000393627.6:c.890T>C	ENSP00000377248.2:p.Ile297Thr
ENST00000469710.5:c.662T>C	ENSP00000418988.1:p.Ile221Thr
ENST00000478741.1:c.750T>C
ENST00000493101.5:c.572T>C	ENSP00000420230.1:p.Ile191Thr
NM_001206924.1:c.572T>C	NP_001193853.1:p.Ile191Thr
NM_001206925.1:c.662T>C	NP_001193854.1:p.Ile221Thr
NM_006889.4:c.890T>C	NP_008820.3:p.Ile297Thr
NM_175862.4:c.908T>C	NP_787058.4:p.Ile303Thr
NM_176892.1:c.746T>C	NP_795711.1:p.Ile249Thr
NM_175862.5:c.908T>C MANE Select	NP_787058.5:p.Ile303Thr
NM_001206924.2:c.572T>C	NP_001193853.2:p.Ile191Thr
NM_001206925.2:c.662T>C	NP_001193854.2:p.Ile221Thr
NM_006889.5:c.890T>C	NP_008820.4:p.Ile297Thr
NM_176892.2:c.746T>C	NP_795711.2:p.Ile249Thr