Canonical Allele Identifier: CA63778622

Gene: CTLA4

Linked Data

• dbSNP Id: rs1030142527
• MyVariant Identifiers: chr2:g.204721707A>G (hg19) ; chr2:g.203856984A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203856984A>G , CM000664.2:g.203856984A>G	GRCh38
NC_000002.11:g.204721707A>G , CM000664.1:g.204721707A>G	GRCh37
NC_000002.10:g.204429952A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.47+2908A>G	ENSP00000512655.1:n.47+2908A>G
XR_923797.1:n.225-5489A>G