Canonical Allele Identifier: CA63778635
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs574719791
gnomAD v3: 2-203857037-C-T
gnomAD v4: 2-203857037-C-T
MyVariant Identifiers: chr2:g.204721760C>T (hg19) chr2:g.203857037C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857037C>T , CM000664.2:g.203857037C>T GRCh38
NC_000002.11:g.204721760C>T , CM000664.1:g.204721760C>T GRCh37
NC_000002.10:g.204430005C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2961C>T ENSP00000512655.1:n.47+2961C>T
XR_923797.1:n.225-5436C>T
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