Canonical Allele Identifier: CA63687115

Gene: CD28

Linked Data

• dbSNP Id: rs572066290
• gnomAD v3: 2-203727208-G-C
• gnomAD v4: 2-203727208-G-C
• MyVariant Identifiers: chr2:g.204591931G>C (hg19) ; chr2:g.203727208G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203727208G>C , CM000664.2:g.203727208G>C	GRCh38
NC_000002.11:g.204591931G>C , CM000664.1:g.204591931G>C	GRCh37
NC_000002.10:g.204300176G>C	NCBI36
NG_029618.1:g.25734G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324106.9:c.409+219G>C MANE Select	ENSP00000324890.7:n.409+219G>C
ENST00000324106.8:c.409+219G>C	ENSP00000324890.7:n.409+219G>C
ENST00000374481.7:c.53-2440G>C	ENSP00000363605.4:n.53-2440G>C
ENST00000458610.6:c.451+219G>C	ENSP00000393648.2:n.451+219G>C
NM_001243077.1:c.118+510G>C	NP_001230006.1:n.118+510G>C
NM_001243078.1:c.53-2440G>C	NP_001230007.1:n.53-2440G>C
NM_006139.3:c.409+219G>C	NP_006130.1:n.409+219G>C
XM_006712862.2:c.133+219G>C	XP_006712925.1:n.133+219G>C
XM_011512194.1:c.451+219G>C	XP_011510496.1:n.451+219G>C
XM_011512195.1:c.199+219G>C	XP_011510497.1:n.199+219G>C
XM_011512196.1:c.160+510G>C	XP_011510498.1:n.160+510G>C
XM_011512197.1:c.157+219G>C	XP_011510499.1:n.157+219G>C
XM_011512194.2:c.451+219G>C	XP_011510496.1:n.451+219G>C
XM_011512195.3:c.199+219G>C	XP_011510497.1:n.199+219G>C
XM_011512197.2:c.157+219G>C	XP_011510499.1:n.157+219G>C
NM_006139.4:c.409+219G>C MANE Select	NP_006130.1:n.409+219G>C
NM_001243077.2:c.118+510G>C	NP_001230006.1:n.118+510G>C
NM_001243078.2:c.53-2440G>C	NP_001230007.1:n.53-2440G>C