Canonical Allele Identifier: CA15195626
Gene: CTLA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1166995
ClinVar RCV Id: RCV001515817
dbSNP Id: rs16840252

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