Canonical Allele Identifier: CA1041457011
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688623530

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866099G>C , CM000664.2:g.203866099G>C GRCh38
NC_000002.11:g.204730822G>C , CM000664.1:g.204730822G>C GRCh37
NC_000002.10:g.204439067G>C NCBI36
NG_011502.1:g.3314G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1819G>C ENSP00000512655.1:n.48-1819G>C