Canonical Allele Identifier: CA763579751

Gene: CTLA4

Linked Data

• dbSNP Id: rs1300488903
• gnomAD v3: 2-203857001-A-C
• gnomAD v4: 2-203857001-A-C
• MyVariant Identifiers: chr2:g.204721724A>C (hg19) ; chr2:g.203857001A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203857001A>C , CM000664.2:g.203857001A>C	GRCh38
NC_000002.11:g.204721724A>C , CM000664.1:g.204721724A>C	GRCh37
NC_000002.10:g.204429969A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.47+2925A>C	ENSP00000512655.1:n.47+2925A>C
XR_923797.1:n.225-5472A>C