Canonical Allele Identifier: CA763579795
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1487376724
gnomAD v3: 2-203857033-G-A
gnomAD v4: 2-203857033-G-A
MyVariant Identifiers: chr2:g.204721756G>A (hg19) chr2:g.203857033G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857033G>A , CM000664.2:g.203857033G>A GRCh38
NC_000002.11:g.204721756G>A , CM000664.1:g.204721756G>A GRCh37
NC_000002.10:g.204430001G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+2957G>A ENSP00000512655.1:n.47+2957G>A
XR_923797.1:n.225-5440G>A
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