Canonical Allele Identifier: CA763579733

Gene: CTLA4

Linked Data

• dbSNP Id: rs1311920395
• MyVariant Identifiers: chr2:g.204721702G>C (hg19) ; chr2:g.203856979G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203856979G>C , CM000664.2:g.203856979G>C	GRCh38
NC_000002.11:g.204721702G>C , CM000664.1:g.204721702G>C	GRCh37
NC_000002.10:g.204429947G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.47+2903G>C	ENSP00000512655.1:n.47+2903G>C
XR_923797.1:n.225-5494G>C