Canonical Allele Identifier: CA763584430

Gene: CTLA4

Linked Data

• dbSNP Id: rs1297661452
• MyVariant Identifiers: chr2:g.204731146C>T (hg19) ; chr2:g.203866423C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203866423C>T , CM000664.2:g.203866423C>T	GRCh38
NC_000002.11:g.204731146C>T , CM000664.1:g.204731146C>T	GRCh37
NC_000002.10:g.204439391C>T	NCBI36
NG_011502.1:g.3638C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.48-1495C>T	ENSP00000512655.1:n.48-1495C>T