Canonical Allele Identifier: CA763579728

Gene: CTLA4

Linked Data

• dbSNP Id: rs1175205939
• gnomAD v3: 2-203856968-G-A
• gnomAD v4: 2-203856968-G-A
• MyVariant Identifiers: chr2:g.204721691G>A (hg19) ; chr2:g.203856968G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203856968G>A , CM000664.2:g.203856968G>A	GRCh38
NC_000002.11:g.204721691G>A , CM000664.1:g.204721691G>A	GRCh37
NC_000002.10:g.204429936G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.47+2892G>A	ENSP00000512655.1:n.47+2892G>A
XR_923797.1:n.225-5505G>A