Canonical Allele Identifier: CA1322144032
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688512902

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203856861G>A , CM000664.2:g.203856861G>A GRCh38
NC_000002.11:g.204721584G>A , CM000664.1:g.204721584G>A GRCh37
NC_000002.10:g.204429829G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2785G>A ENSP00000512655.1:n.47+2785G>A
XR_923797.1:n.225-5612G>A