Canonical Allele Identifier: CA1041457153
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688629487

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866391A>G , CM000664.2:g.203866391A>G GRCh38
NC_000002.11:g.204731114A>G , CM000664.1:g.204731114A>G GRCh37
NC_000002.10:g.204439359A>G NCBI36
NG_011502.1:g.3606A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.48-1527A>G ENSP00000512655.1:n.48-1527A>G