Canonical Allele Identifier: CA2701510671

Gene: CD28

Linked Data

• dbSNP Id: rs2106120480

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203727329G>T , CM000664.2:g.203727329G>T	GRCh38
NC_000002.11:g.204592052G>T , CM000664.1:g.204592052G>T	GRCh37
NC_000002.10:g.204300297G>T	NCBI36
NG_029618.1:g.25855G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324106.9:c.409+340G>T MANE Select	ENSP00000324890.7:n.409+340G>T
ENST00000324106.8:c.409+340G>T	ENSP00000324890.7:n.409+340G>T
ENST00000374481.7:c.53-2319G>T	ENSP00000363605.4:n.53-2319G>T
ENST00000458610.6:c.451+340G>T	ENSP00000393648.2:n.451+340G>T
NM_001243077.1:c.118+631G>T	NP_001230006.1:n.118+631G>T
NM_001243078.1:c.53-2319G>T	NP_001230007.1:n.53-2319G>T
NM_006139.3:c.409+340G>T	NP_006130.1:n.409+340G>T
XM_006712862.2:c.133+340G>T	XP_006712925.1:n.133+340G>T
XM_011512194.1:c.451+340G>T	XP_011510496.1:n.451+340G>T
XM_011512195.1:c.199+340G>T	XP_011510497.1:n.199+340G>T
XM_011512196.1:c.160+631G>T	XP_011510498.1:n.160+631G>T
XM_011512197.1:c.157+340G>T	XP_011510499.1:n.157+340G>T
XM_011512194.2:c.451+340G>T	XP_011510496.1:n.451+340G>T
XM_011512195.3:c.199+340G>T	XP_011510497.1:n.199+340G>T
XM_011512197.2:c.157+340G>T	XP_011510499.1:n.157+340G>T
NM_006139.4:c.409+340G>T MANE Select	NP_006130.1:n.409+340G>T
NM_001243077.2:c.118+631G>T	NP_001230006.1:n.118+631G>T
NM_001243078.2:c.53-2319G>T	NP_001230007.1:n.53-2319G>T