Canonical Allele Identifier: CA63778555
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1013771077
gnomAD v2: 2-204721526-C-T
gnomAD v3: 2-203856803-C-T
gnomAD v4: 2-203856803-C-T
MyVariant Identifiers: chr2:g.204721526C>T (hg19) chr2:g.203856803C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203856803C>T , CM000664.2:g.203856803C>T GRCh38
NC_000002.11:g.204721526C>T , CM000664.1:g.204721526C>T GRCh37
NC_000002.10:g.204429771C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+2727C>T ENSP00000512655.1:n.47+2727C>T
XR_923797.1:n.225-5670C>T
Search 100 bp 5'
Search 100 bp 3'