Canonical Allele Identifier: CA763584367
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1358678352
gnomAD v3: 2-203866330-G-A
gnomAD v4: 2-203866330-G-A
MyVariant Identifiers: chr2:g.204731053G>A (hg19) chr2:g.203866330G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866330G>A , CM000664.2:g.203866330G>A GRCh38
NC_000002.11:g.204731053G>A , CM000664.1:g.204731053G>A GRCh37
NC_000002.10:g.204439298G>A NCBI36
NG_011502.1:g.3545G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.48-1588G>A ENSP00000512655.1:n.48-1588G>A
Search 100 bp 5'
Search 100 bp 3'