Canonical Allele Identifier: CA63778620

Gene: CTLA4

Linked Data

• dbSNP Id: rs867582821
• gnomAD v3: 2-203856969-C-T
• gnomAD v4: 2-203856969-C-T
• MyVariant Identifiers: chr2:g.204721692C>T (hg19) ; chr2:g.203856969C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203856969C>T , CM000664.2:g.203856969C>T	GRCh38
NC_000002.11:g.204721692C>T , CM000664.1:g.204721692C>T	GRCh37
NC_000002.10:g.204429937C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.47+2893C>T	ENSP00000512655.1:n.47+2893C>T
XR_923797.1:n.225-5504C>T