Canonical Allele Identifier: CA63683323
Gene: CD28 HGNC NCBI

Linked Data

dbSNP Id: rs3116487

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203721314C>A , CM000664.2:g.203721314C>A GRCh38
NC_000002.11:g.204586037C>A , CM000664.1:g.204586037C>A GRCh37
NC_000002.10:g.204294282C>A NCBI36
NG_029618.1:g.19840C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000324106.9:c.53-5319C>A MANE Select ENSP00000324890.7:n.53-5319C>A
ENST00000324106.8:c.53-5319C>A ENSP00000324890.7:n.53-5319C>A
ENST00000374481.7:c.53-8334C>A ENSP00000363605.4:n.53-8334C>A
ENST00000458610.6:c.95-5319C>A ENSP00000393648.2:n.95-5319C>A
NM_001243077.1:c.53-5319C>A NP_001230006.1:n.53-5319C>A
NM_001243078.1:c.53-8334C>A NP_001230007.1:n.53-8334C>A
NM_006139.3:c.53-5319C>A NP_006130.1:n.53-5319C>A
XM_006712862.2:c.95-5637C>A XP_006712925.1:n.95-5637C>A
XM_011512194.1:c.95-5319C>A XP_011510496.1:n.95-5319C>A
XM_011512195.1:c.95-5319C>A XP_011510497.1:n.95-5319C>A
XM_011512196.1:c.95-5319C>A XP_011510498.1:n.95-5319C>A
XM_011512197.1:c.53-5319C>A XP_011510499.1:n.53-5319C>A
XM_011512194.2:c.95-5319C>A XP_011510496.1:n.95-5319C>A
XM_011512195.3:c.95-5319C>A XP_011510497.1:n.95-5319C>A
XM_011512197.2:c.53-5319C>A XP_011510499.1:n.53-5319C>A
NM_006139.4:c.53-5319C>A MANE Select NP_006130.1:n.53-5319C>A
NM_001243077.2:c.53-5319C>A NP_001230006.1:n.53-5319C>A
NM_001243078.2:c.53-8334C>A NP_001230007.1:n.53-8334C>A