Canonical Allele Identifier: CA763579780
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1426013931
MyVariant Identifiers: chr2:g.204721741A>G (hg19) chr2:g.203857018A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857018A>G , CM000664.2:g.203857018A>G GRCh38
NC_000002.11:g.204721741A>G , CM000664.1:g.204721741A>G GRCh37
NC_000002.10:g.204429986A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2942A>G ENSP00000512655.1:n.47+2942A>G
XR_923797.1:n.225-5455A>G
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