Canonical Allele Identifier: CA63784464
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs733618

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866221T>C , CM000664.2:g.203866221T>C GRCh38
NC_000002.11:g.204730944T>C , CM000664.1:g.204730944T>C GRCh37
NC_000002.10:g.204439189T>C NCBI36
NG_011502.1:g.3436T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.48-1697T>C ENSP00000512655.1:n.48-1697T>C