Canonical Allele Identifier: CA63778760

Gene: CTLA4

Linked Data

• dbSNP Id: rs1007641253
• MyVariant Identifiers: chr2:g.204721984T>G (hg19) ; chr2:g.203857261T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203857261T>G , CM000664.2:g.203857261T>G	GRCh38
NC_000002.11:g.204721984T>G , CM000664.1:g.204721984T>G	GRCh37
NC_000002.10:g.204430229T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696479.1:c.47+3185T>G	ENSP00000512655.1:n.47+3185T>G
XR_923797.1:n.225-5212T>G