Canonical Allele Identifier: CA63784553
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs188607442
gnomAD v2: 2-204731069-G-A
gnomAD v3: 2-203866346-G-A
gnomAD v4: 2-203866346-G-A
MyVariant Identifiers: chr2:g.204731069G>A (hg19) chr2:g.203866346G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866346G>A , CM000664.2:g.203866346G>A GRCh38
NC_000002.11:g.204731069G>A , CM000664.1:g.204731069G>A GRCh37
NC_000002.10:g.204439314G>A NCBI36
NG_011502.1:g.3561G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.48-1572G>A ENSP00000512655.1:n.48-1572G>A
Search 100 bp 5'
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