Canonical Allele Identifier: CA1322147778
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688622528

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866049C>A , CM000664.2:g.203866049C>A GRCh38
NC_000002.11:g.204730772C>A , CM000664.1:g.204730772C>A GRCh37
NC_000002.10:g.204439017C>A NCBI36
NG_011502.1:g.3264C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1869C>A ENSP00000512655.1:n.48-1869C>A