Canonical Allele Identifier: CA763584346

Gene: CTLA4

Linked Data

• dbSNP Id: rs1238942810
• gnomAD v3: 2-203866281-T-A
• gnomAD v4: 2-203866281-T-A
• MyVariant Identifiers: chr2:g.204731004T>A (hg19) ; chr2:g.203866281T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203866281T>A , CM000664.2:g.203866281T>A	GRCh38
NC_000002.11:g.204731004T>A , CM000664.1:g.204731004T>A	GRCh37
NC_000002.10:g.204439249T>A	NCBI36
NG_011502.1:g.3496T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696479.1:c.48-1637T>A	ENSP00000512655.1:n.48-1637T>A