Canonical Allele Identifier: CA763584314

Gene: CTLA4

Linked Data

• dbSNP Id: rs1359026702
• gnomAD v3: 2-203866197-C-G
• gnomAD v4: 2-203866197-C-G
• MyVariant Identifiers: chr2:g.204730920C>G (hg19) ; chr2:g.203866197C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203866197C>G , CM000664.2:g.203866197C>G	GRCh38
NC_000002.11:g.204730920C>G , CM000664.1:g.204730920C>G	GRCh37
NC_000002.10:g.204439165C>G	NCBI36
NG_011502.1:g.3412C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696479.1:c.48-1721C>G	ENSP00000512655.1:n.48-1721C>G