Canonical Allele Identifier: CA763579816

Gene: CTLA4

Linked Data

• dbSNP Id: rs1319873892
• gnomAD v3: 2-203857079-C-CT
• gnomAD v4: 2-203857079-C-CT
• MyVariant Identifiers: chr2:g.204721802_204721803insT (hg19) ; chr2:g.203857079_203857080insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203857085dup , CM000664.2:g.203857085dup	GRCh38
NC_000002.11:g.204721808dup , CM000664.1:g.204721808dup	GRCh37
NC_000002.10:g.204430053dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696479.1:c.47+3009dup	ENSP00000512655.1:n.47+3009dup
XR_923797.1:n.225-5388dup