Canonical Allele Identifier: CA63778630

Gene: CTLA4

Linked Data

• dbSNP Id: rs986650504
• gnomAD v3: 2-203857005-A-G
• gnomAD v4: 2-203857005-A-G
• MyVariant Identifiers: chr2:g.204721728A>G (hg19) ; chr2:g.203857005A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203857005A>G , CM000664.2:g.203857005A>G	GRCh38
NC_000002.11:g.204721728A>G , CM000664.1:g.204721728A>G	GRCh37
NC_000002.10:g.204429973A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.47+2929A>G	ENSP00000512655.1:n.47+2929A>G
XR_923797.1:n.225-5468A>G