Canonical Allele Identifier: CA1322144167
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857195T= , CM000664.2:g.203857195T= GRCh38
NC_000002.11:g.204721918T= , CM000664.1:g.204721918T= GRCh37
NC_000002.10:g.204430163T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+3119T= ENSP00000512655.1:n.47+3119T=
XR_923797.1:n.225-5278T=