Canonical Allele Identifier: CA763579715

Gene: CTLA4

Linked Data

• dbSNP Id: rs1216175634
• gnomAD v3: 2-203856963-T-TA
• gnomAD v4: 2-203856963-T-TA
• MyVariant Identifiers: chr2:g.204721686_204721687insA (hg19) ; chr2:g.203856963_203856964insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203856966dup , CM000664.2:g.203856966dup	GRCh38
NC_000002.11:g.204721689dup , CM000664.1:g.204721689dup	GRCh37
NC_000002.10:g.204429934dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.47+2890dup	ENSP00000512655.1:n.47+2890dup
XR_923797.1:n.225-5507dup