Canonical Allele Identifier: CA1322144091
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857018A= , CM000664.2:g.203857018A= GRCh38
NC_000002.11:g.204721741A= , CM000664.1:g.204721741A= GRCh37
NC_000002.10:g.204429986A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2942A= ENSP00000512655.1:n.47+2942A=
XR_923797.1:n.225-5455A=