Canonical Allele Identifier: CA435252274

Gene: CD86

Linked Data

• MyVariant Identifiers: chr3:g.121838327T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119480T>C , CM000665.2:g.122119480T>C	GRCh38
NC_000003.11:g.121838327T>C , CM000665.1:g.121838327T>C	GRCh37
NC_000003.10:g.123321017T>C	NCBI36
NG_029928.1:g.69119T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.936T>C MANE Select	ENSP00000332049.2:p.Arg312=
ENST00000264468.9:c.774T>C	ENSP00000264468.6:p.Arg258=
ENST00000330540.6:c.936T>C	ENSP00000332049.2:p.Arg312=
ENST00000393627.6:c.918T>C	ENSP00000377248.2:p.Arg306=
ENST00000469710.5:c.690T>C	ENSP00000418988.1:p.Arg230=
ENST00000478741.1:c.778T>C
ENST00000493101.5:c.600T>C	ENSP00000420230.1:p.Arg200=
NM_001206924.1:c.600T>C	NP_001193853.1:p.Arg200=
NM_001206925.1:c.690T>C	NP_001193854.1:p.Arg230=
NM_006889.4:c.918T>C	NP_008820.3:p.Arg306=
NM_175862.4:c.936T>C	NP_787058.4:p.Arg312=
NM_176892.1:c.774T>C	NP_795711.1:p.Arg258=
NM_175862.5:c.936T>C MANE Select	NP_787058.5:p.Arg312=
NM_001206924.2:c.600T>C	NP_001193853.2:p.Arg200=
NM_001206925.2:c.690T>C	NP_001193854.2:p.Arg230=
NM_006889.5:c.918T>C	NP_008820.4:p.Arg306=
NM_176892.2:c.774T>C	NP_795711.2:p.Arg258=