Canonical Allele Identifier: CA1041457113
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688628045

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866319C>T , CM000664.2:g.203866319C>T GRCh38
NC_000002.11:g.204731042C>T , CM000664.1:g.204731042C>T GRCh37
NC_000002.10:g.204439287C>T NCBI36
NG_011502.1:g.3534C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1599C>T ENSP00000512655.1:n.48-1599C>T