Canonical Allele Identifier: CA539148601
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1305794005

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866430C>G , CM000664.2:g.203866430C>G GRCh38
NC_000002.11:g.204731153C>G , CM000664.1:g.204731153C>G GRCh37
NC_000002.10:g.204439398C>G NCBI36
NG_011502.1:g.3645C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1488C>G ENSP00000512655.1:n.48-1488C>G