Canonical Allele Identifier: CA1322144059
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203856935A= , CM000664.2:g.203856935A= GRCh38
NC_000002.11:g.204721658A= , CM000664.1:g.204721658A= GRCh37
NC_000002.10:g.204429903A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+2859A= ENSP00000512655.1:n.47+2859A=
XR_923797.1:n.225-5538A=