Canonical Allele Identifier: CA1322144098
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857030A= , CM000664.2:g.203857030A= GRCh38
NC_000002.11:g.204721753A= , CM000664.1:g.204721753A= GRCh37
NC_000002.10:g.204429998A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2954A= ENSP00000512655.1:n.47+2954A=
XR_923797.1:n.225-5443A=