Canonical Allele Identifier: CA1322147796
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688623230

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866088A>C , CM000664.2:g.203866088A>C GRCh38
NC_000002.11:g.204730811A>C , CM000664.1:g.204730811A>C GRCh37
NC_000002.10:g.204439056A>C NCBI36
NG_011502.1:g.3303A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1830A>C ENSP00000512655.1:n.48-1830A>C