Canonical Allele Identifier: CA63778809
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs772439387
MyVariant Identifiers: chr2:g.204722054T>G (hg19) chr2:g.203857331T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857331T>G , CM000664.2:g.203857331T>G GRCh38
NC_000002.11:g.204722054T>G , CM000664.1:g.204722054T>G GRCh37
NC_000002.10:g.204430299T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+3255T>G ENSP00000512655.1:n.47+3255T>G
XR_923797.1:n.225-5142T>G
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