Canonical Allele Identifier: CA539147725
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1240240812
gnomAD v2: 2-204721550-A-G
gnomAD v3: 2-203856827-A-G
gnomAD v4: 2-203856827-A-G
MyVariant Identifiers: chr2:g.204721550A>G (hg19) chr2:g.203856827A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203856827A>G , CM000664.2:g.203856827A>G GRCh38
NC_000002.11:g.204721550A>G , CM000664.1:g.204721550A>G GRCh37
NC_000002.10:g.204429795A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+2751A>G ENSP00000512655.1:n.47+2751A>G
XR_923797.1:n.225-5646A>G
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