Canonical Allele Identifier: CA11292057

Gene: CTLA4

Linked Data

• dbSNP Id: rs4553808
• gnomAD v2: 2-204731005-A-G
• gnomAD v3: 2-203866282-A-G
• gnomAD v4: 2-203866282-A-G
• MyVariant Identifiers: chr2:g.204731005A>G (hg19) ; chr2:g.203866282A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203866282A>G , CM000664.2:g.203866282A>G	GRCh38
NC_000002.11:g.204731005A>G , CM000664.1:g.204731005A>G	GRCh37
NC_000002.10:g.204439250A>G	NCBI36
NG_011502.1:g.3497A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.48-1636A>G	ENSP00000512655.1:n.48-1636A>G