Canonical Allele Identifier: CA1322147969
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866433A= , CM000664.2:g.203866433A= GRCh38
NC_000002.11:g.204731156A= , CM000664.1:g.204731156A= GRCh37
NC_000002.10:g.204439401A= NCBI36
NG_011502.1:g.3648A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1485A= ENSP00000512655.1:n.48-1485A=