Canonical Allele Identifier: CA1322144170
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688516466

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857205A>C , CM000664.2:g.203857205A>C GRCh38
NC_000002.11:g.204721928A>C , CM000664.1:g.204721928A>C GRCh37
NC_000002.10:g.204430173A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+3129A>C ENSP00000512655.1:n.47+3129A>C
XR_923797.1:n.225-5268A>C