Canonical Allele Identifier: CA63786570
Gene: CTLA4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs35219727

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203869326G>A , CM000664.2:g.203869326G>A GRCh38
NC_000002.11:g.204734049G>A , CM000664.1:g.204734049G>A GRCh37
NC_000002.10:g.204442294G>A NCBI36
NG_011502.1:g.6541G>A

Transcript Alleles

HGVS Amino-acid change
NM_001037631.2:c.110-1260G>A VV NP_001032720.1:p.=
NM_005214.4:c.110-1260G>A VV NP_005205.2:p.=
XR_241294.1:n.250-1260G>A
NM_001037631.3:c.110-1260G>A VV NP_001032720.1:p.=
NM_005214.5:c.110-1260G>A VV NP_005205.2:p.=
ENST00000295854.10:n.110-1260G>A ENSP00000295854.6:p.=
ENST00000302823.7:c.110-1260G>A ENSP00000303939.3:p.=
ENST00000472206.1:n.110-1260G>A ENSP00000417779.1:p.=
ENST00000487393.1:n.109+1275G>A