Canonical Allele Identifier: CA1322144089
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688514452

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857007T>C , CM000664.2:g.203857007T>C GRCh38
NC_000002.11:g.204721730T>C , CM000664.1:g.204721730T>C GRCh37
NC_000002.10:g.204429975T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2931T>C ENSP00000512655.1:n.47+2931T>C
XR_923797.1:n.225-5466T>C