Canonical Allele Identifier: CA763579875

Gene: CTLA4

Linked Data

• dbSNP Id: rs1170857191
• gnomAD v3: 2-203857271-G-T
• gnomAD v4: 2-203857271-G-T
• MyVariant Identifiers: chr2:g.204721994G>T (hg19) ; chr2:g.203857271G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203857271G>T , CM000664.2:g.203857271G>T	GRCh38
NC_000002.11:g.204721994G>T , CM000664.1:g.204721994G>T	GRCh37
NC_000002.10:g.204430239G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696479.1:c.47+3195G>T	ENSP00000512655.1:n.47+3195G>T
XR_923797.1:n.225-5202G>T