Canonical Allele Identifier: CA1041457173
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688629710

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866399G>A , CM000664.2:g.203866399G>A GRCh38
NC_000002.11:g.204731122G>A , CM000664.1:g.204731122G>A GRCh37
NC_000002.10:g.204439367G>A NCBI36
NG_011502.1:g.3614G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.48-1519G>A ENSP00000512655.1:n.48-1519G>A