Canonical Allele Identifier: CA763584239
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1296148321
MyVariant Identifiers: chr2:g.204730775C>T (hg19) chr2:g.203866052C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866052C>T , CM000664.2:g.203866052C>T GRCh38
NC_000002.11:g.204730775C>T , CM000664.1:g.204730775C>T GRCh37
NC_000002.10:g.204439020C>T NCBI36
NG_011502.1:g.3267C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1866C>T ENSP00000512655.1:n.48-1866C>T
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