Canonical Allele Identifier: CA1322144137
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688515751

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857124A>G , CM000664.2:g.203857124A>G GRCh38
NC_000002.11:g.204721847A>G , CM000664.1:g.204721847A>G GRCh37
NC_000002.10:g.204430092A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+3048A>G ENSP00000512655.1:n.47+3048A>G
XR_923797.1:n.225-5349A>G