Canonical Allele Identifier: CA63784625
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs958666804

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866431C>A , CM000664.2:g.203866431C>A GRCh38
NC_000002.11:g.204731154C>A , CM000664.1:g.204731154C>A GRCh37
NC_000002.10:g.204439399C>A NCBI36
NG_011502.1:g.3646C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1487C>A ENSP00000512655.1:n.48-1487C>A