Canonical Allele Identifier: CA763579890

Gene: CTLA4

Linked Data

• dbSNP Id: rs1458106388
• gnomAD v3: 2-203857345-A-AT
• gnomAD v4: 2-203857345-A-AT
• MyVariant Identifiers: chr2:g.204722068_204722069insT (hg19) ; chr2:g.203857345_203857346insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203857352dup , CM000664.2:g.203857352dup	GRCh38
NC_000002.11:g.204722075dup , CM000664.1:g.204722075dup	GRCh37
NC_000002.10:g.204430320dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696479.1:c.47+3276dup	ENSP00000512655.1:n.47+3276dup
XR_923797.1:n.225-5121dup