Canonical Allele Identifier: CA63683404

Gene: CD28

Linked Data

• dbSNP Id: rs933395071
• gnomAD v3: 2-203721351-A-G
• gnomAD v4: 2-203721351-A-G
• MyVariant Identifiers: chr2:g.204586074A>G (hg19) ; chr2:g.203721351A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203721351A>G , CM000664.2:g.203721351A>G	GRCh38
NC_000002.11:g.204586074A>G , CM000664.1:g.204586074A>G	GRCh37
NC_000002.10:g.204294319A>G	NCBI36
NG_029618.1:g.19877A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324106.9:c.53-5282A>G MANE Select	ENSP00000324890.7:n.53-5282A>G
ENST00000324106.8:c.53-5282A>G	ENSP00000324890.7:n.53-5282A>G
ENST00000374481.7:c.53-8297A>G	ENSP00000363605.4:n.53-8297A>G
ENST00000458610.6:c.95-5282A>G	ENSP00000393648.2:n.95-5282A>G
NM_001243077.1:c.53-5282A>G	NP_001230006.1:n.53-5282A>G
NM_001243078.1:c.53-8297A>G	NP_001230007.1:n.53-8297A>G
NM_006139.3:c.53-5282A>G	NP_006130.1:n.53-5282A>G
XM_006712862.2:c.95-5600A>G	XP_006712925.1:n.95-5600A>G
XM_011512194.1:c.95-5282A>G	XP_011510496.1:n.95-5282A>G
XM_011512195.1:c.95-5282A>G	XP_011510497.1:n.95-5282A>G
XM_011512196.1:c.95-5282A>G	XP_011510498.1:n.95-5282A>G
XM_011512197.1:c.53-5282A>G	XP_011510499.1:n.53-5282A>G
XM_011512194.2:c.95-5282A>G	XP_011510496.1:n.95-5282A>G
XM_011512195.3:c.95-5282A>G	XP_011510497.1:n.95-5282A>G
XM_011512197.2:c.53-5282A>G	XP_011510499.1:n.53-5282A>G
NM_006139.4:c.53-5282A>G MANE Select	NP_006130.1:n.53-5282A>G
NM_001243077.2:c.53-5282A>G	NP_001230006.1:n.53-5282A>G
NM_001243078.2:c.53-8297A>G	NP_001230007.1:n.53-8297A>G