Canonical Allele Identifier: CA1041453170
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688513314
gnomAD v3: 2-203856906-G-T
gnomAD v4: 2-203856906-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203856906G>T , CM000664.2:g.203856906G>T GRCh38
NC_000002.11:g.204721629G>T , CM000664.1:g.204721629G>T GRCh37
NC_000002.10:g.204429874G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2830G>T ENSP00000512655.1:n.47+2830G>T
XR_923797.1:n.225-5567G>T
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