Canonical Allele Identifier: CA1322147779
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866052C= , CM000664.2:g.203866052C= GRCh38
NC_000002.11:g.204730775C= , CM000664.1:g.204730775C= GRCh37
NC_000002.10:g.204439020C= NCBI36
NG_011502.1:g.3267C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1866C= ENSP00000512655.1:n.48-1866C=