Canonical Allele Identifier: CA63778626
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs924475695
gnomAD v2: 2-204721716-TATCA-T
gnomAD v3: 2-203856993-TATCA-T
gnomAD v4: 2-203856993-TATCA-T
MyVariant Identifiers: chr2:g.204721717_204721720del (hg19) chr2:g.203856994_203856997del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857004_203857007del , CM000664.2:g.203857004_203857007del GRCh38
NC_000002.11:g.204721727_204721730del , CM000664.1:g.204721727_204721730del GRCh37
NC_000002.10:g.204429972_204429975del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2928_47+2931del ENSP00000512655.1:n.47+2928_47+2931del
XR_923797.1:n.225-5469_225-5466del
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