Canonical Allele Identifier: CA763579874

Gene: CTLA4

Linked Data

• dbSNP Id: rs1398738164
• MyVariant Identifiers: chr2:g.204721993_204721996del (hg19) ; chr2:g.203857270_203857273del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203857270_203857273del , CM000664.2:g.203857270_203857273del	GRCh38
NC_000002.11:g.204721993_204721996del , CM000664.1:g.204721993_204721996del	GRCh37
NC_000002.10:g.204430238_204430241del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696479.1:c.47+3194_47+3197del	ENSP00000512655.1:n.47+3194_47+3197del
XR_923797.1:n.225-5203_225-5200del