Canonical Allele Identifier: CA1322147792
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866085A= , CM000664.2:g.203866085A= GRCh38
NC_000002.11:g.204730808A= , CM000664.1:g.204730808A= GRCh37
NC_000002.10:g.204439053A= NCBI36
NG_011502.1:g.3300A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1833A= ENSP00000512655.1:n.48-1833A=