Canonical Allele Identifier: CA63778738
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs386654296
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857238_203857239delinsCT , CM000664.2:g.203857238_203857239delinsCT GRCh38
NC_000002.11:g.204721961_204721962delinsCT , CM000664.1:g.204721961_204721962delinsCT GRCh37
NC_000002.10:g.204430206_204430207delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+3162_47+3163delinsCT ENSP00000512655.1:n.47+3162_47+3163delinsCT
XR_923797.1:n.225-5235_225-5234delinsCT
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