Canonical Allele Identifier: CA539147726
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1167979468
gnomAD v2: 2-204721611-A-G
gnomAD v3: 2-203856888-A-G
gnomAD v4: 2-203856888-A-G
MyVariant Identifiers: chr2:g.204721611A>G (hg19) chr2:g.203856888A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203856888A>G , CM000664.2:g.203856888A>G GRCh38
NC_000002.11:g.204721611A>G , CM000664.1:g.204721611A>G GRCh37
NC_000002.10:g.204429856A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2812A>G ENSP00000512655.1:n.47+2812A>G
XR_923797.1:n.225-5585A>G
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