Canonical Allele Identifier: CA1322143985
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688511252

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203856738G>A , CM000664.2:g.203856738G>A GRCh38
NC_000002.11:g.204721461G>A , CM000664.1:g.204721461G>A GRCh37
NC_000002.10:g.204429706G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+2662G>A ENSP00000512655.1:n.47+2662G>A
XR_923797.1:n.225-5735G>A