Canonical Allele Identifier: CA763584217

Gene: CTLA4

Linked Data

• dbSNP Id: rs1317238872
• gnomAD v3: 2-203866042-T-C
• gnomAD v4: 2-203866042-T-C
• MyVariant Identifiers: chr2:g.204730765T>C (hg19) ; chr2:g.203866042T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203866042T>C , CM000664.2:g.203866042T>C	GRCh38
NC_000002.11:g.204730765T>C , CM000664.1:g.204730765T>C	GRCh37
NC_000002.10:g.204439010T>C	NCBI36
NG_011502.1:g.3257T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696479.1:c.48-1876T>C	ENSP00000512655.1:n.48-1876T>C