Canonical Allele Identifier: CA11095292

Gene: CTLA4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203866366G>A , CM000664.2:g.203866366G>A	GRCh38
NC_000002.11:g.204731089G>A , CM000664.1:g.204731089G>A	GRCh37
NC_000002.10:g.204439334G>A	NCBI36
NG_011502.1:g.3581G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696479.1:c.48-1552G>A	ENSP00000512655.1:n.48-1552G>A