Canonical Allele Identifier: CA63784572

Gene: CTLA4

Linked Data

• dbSNP Id: rs115552468
• gnomAD v2: 2-204731128-T-A
• gnomAD v3: 2-203866405-T-A
• gnomAD v4: 2-203866405-T-A
• MyVariant Identifiers: chr2:g.204731128T>A (hg19) ; chr2:g.203866405T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203866405T>A , CM000664.2:g.203866405T>A	GRCh38
NC_000002.11:g.204731128T>A , CM000664.1:g.204731128T>A	GRCh37
NC_000002.10:g.204439373T>A	NCBI36
NG_011502.1:g.3620T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.48-1513T>A	ENSP00000512655.1:n.48-1513T>A