Canonical Allele Identifier: CA435252255

Gene: CD86

Linked Data

• gnomAD v4: 3-122119447-C-A
• COSMIC: COSM4956770
• MyVariant Identifiers: chr3:g.121838294C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119447C>A , CM000665.2:g.122119447C>A	GRCh38
NC_000003.11:g.121838294C>A , CM000665.1:g.121838294C>A	GRCh37
NC_000003.10:g.123320984C>A	NCBI36
NG_029928.1:g.69086C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.903C>A MANE Select	ENSP00000332049.2:p.Ile301=
ENST00000264468.9:c.741C>A	ENSP00000264468.6:p.Ile247=
ENST00000330540.6:c.903C>A	ENSP00000332049.2:p.Ile301=
ENST00000393627.6:c.885C>A	ENSP00000377248.2:p.Ile295=
ENST00000469710.5:c.657C>A	ENSP00000418988.1:p.Ile219=
ENST00000478741.1:c.745C>A
ENST00000493101.5:c.567C>A	ENSP00000420230.1:p.Ile189=
NM_001206924.1:c.567C>A	NP_001193853.1:p.Ile189=
NM_001206925.1:c.657C>A	NP_001193854.1:p.Ile219=
NM_006889.4:c.885C>A	NP_008820.3:p.Ile295=
NM_175862.4:c.903C>A	NP_787058.4:p.Ile301=
NM_176892.1:c.741C>A	NP_795711.1:p.Ile247=
NM_175862.5:c.903C>A MANE Select	NP_787058.5:p.Ile301=
NM_001206924.2:c.567C>A	NP_001193853.2:p.Ile189=
NM_001206925.2:c.657C>A	NP_001193854.2:p.Ile219=
NM_006889.5:c.885C>A	NP_008820.4:p.Ile295=
NM_176892.2:c.741C>A	NP_795711.2:p.Ile247=