Canonical Allele Identifier: CA63778649
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs924823530
gnomAD v3: 2-203857076-G-A
gnomAD v4: 2-203857076-G-A
COSMIC: COSN6933206
MyVariant Identifiers: chr2:g.204721799G>A (hg19) chr2:g.203857076G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857076G>A , CM000664.2:g.203857076G>A GRCh38
NC_000002.11:g.204721799G>A , CM000664.1:g.204721799G>A GRCh37
NC_000002.10:g.204430044G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+3000G>A ENSP00000512655.1:n.47+3000G>A
XR_923797.1:n.225-5397G>A
Search 100 bp 5'
Search 100 bp 3'