Canonical Allele Identifier: CA1041453367
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1321782302
gnomAD v3: 2-203857353-C-A
gnomAD v4: 2-203857353-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857353C>A , CM000664.2:g.203857353C>A GRCh38
NC_000002.11:g.204722076C>A , CM000664.1:g.204722076C>A GRCh37
NC_000002.10:g.204430321C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+3277C>A ENSP00000512655.1:n.47+3277C>A
XR_923797.1:n.225-5120C>A
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