Canonical Allele Identifier: CA763584258
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1424994359
MyVariant Identifiers: chr2:g.204730808A>G (hg19) chr2:g.203866085A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866085A>G , CM000664.2:g.203866085A>G GRCh38
NC_000002.11:g.204730808A>G , CM000664.1:g.204730808A>G GRCh37
NC_000002.10:g.204439053A>G NCBI36
NG_011502.1:g.3300A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1833A>G ENSP00000512655.1:n.48-1833A>G
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