Canonical Allele Identifier: CA63784641
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs773751715

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866450A>G , CM000664.2:g.203866450A>G GRCh38
NC_000002.11:g.204731173A>G , CM000664.1:g.204731173A>G GRCh37
NC_000002.10:g.204439418A>G NCBI36
NG_011502.1:g.3665A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1468A>G ENSP00000512655.1:n.48-1468A>G