Canonical Allele Identifier: CA1322147881
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866274C= , CM000664.2:g.203866274C= GRCh38
NC_000002.11:g.204730997C= , CM000664.1:g.204730997C= GRCh37
NC_000002.10:g.204439242C= NCBI36
NG_011502.1:g.3489C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.48-1644C= ENSP00000512655.1:n.48-1644C=