Canonical Allele Identifier: CA63778624

Gene: CTLA4

Linked Data

• dbSNP Id: rs190670063
• gnomAD v2: 2-204721708-A-G
• gnomAD v3: 2-203856985-A-G
• gnomAD v4: 2-203856985-A-G
• MyVariant Identifiers: chr2:g.204721708A>G (hg19) ; chr2:g.203856985A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203856985A>G , CM000664.2:g.203856985A>G	GRCh38
NC_000002.11:g.204721708A>G , CM000664.1:g.204721708A>G	GRCh37
NC_000002.10:g.204429953A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.47+2909A>G	ENSP00000512655.1:n.47+2909A>G
XR_923797.1:n.225-5488A>G