Canonical Allele Identifier: CA763579761
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1456685090
gnomAD v3: 2-203857003-T-C
gnomAD v4: 2-203857003-T-C
MyVariant Identifiers: chr2:g.204721726T>C (hg19) chr2:g.203857003T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857003T>C , CM000664.2:g.203857003T>C GRCh38
NC_000002.11:g.204721726T>C , CM000664.1:g.204721726T>C GRCh37
NC_000002.10:g.204429971T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2927T>C ENSP00000512655.1:n.47+2927T>C
XR_923797.1:n.225-5470T>C
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