Canonical Allele Identifier: CA63784506

Gene: CTLA4

Linked Data

• dbSNP Id: rs944464998
• MyVariant Identifiers: chr2:g.204730997C>T (hg19) ; chr2:g.203866274C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203866274C>T , CM000664.2:g.203866274C>T	GRCh38
NC_000002.11:g.204730997C>T , CM000664.1:g.204730997C>T	GRCh37
NC_000002.10:g.204439242C>T	NCBI36
NG_011502.1:g.3489C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696479.1:c.48-1644C>T	ENSP00000512655.1:n.48-1644C>T