Canonical Allele Identifier: CA15195626
Gene: CTLA4 HGNC NCBI
MyVariant.info:
GRCh38 chr2:g.203866796C>T
GRCh37 chr2:g.204731519C>T
gnomAD v2:
2:204731519 C / T
gnomAD v3:
2:203866796 C / T
gnomAD v4:
chr2-203866796-C-T
Joint Max Group AF 0.17163587 (NFE)
Genomes Max Group AF 0.17163587 (NFE)
ClinVar RCV:
RCV001515817
ClinVar Variation:
1166995
dbSNP:
16840252
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866796C>T , CM000664.2:g.203866796C>T GRCh38
NC_000002.11:g.204731519C>T , CM000664.1:g.204731519C>T GRCh37
NC_000002.10:g.204439764C>T NCBI36
NG_011502.1:g.4011C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1122C>T ENSP00000512655.1:n.48-1122C>T
Search 100 bp 5'
Search 100 bp 3'