Canonical Allele Identifier: CA539148579
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1266751177

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866226C>T , CM000664.2:g.203866226C>T GRCh38
NC_000002.11:g.204730949C>T , CM000664.1:g.204730949C>T GRCh37
NC_000002.10:g.204439194C>T NCBI36
NG_011502.1:g.3441C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.48-1692C>T ENSP00000512655.1:n.48-1692C>T