Canonical Allele Identifier: CA63778580
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs553900646
gnomAD v2: 2-204721593-C-T
gnomAD v3: 2-203856870-C-T
gnomAD v4: 2-203856870-C-T
MyVariant Identifiers: chr2:g.204721593C>T (hg19) chr2:g.203856870C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203856870C>T , CM000664.2:g.203856870C>T GRCh38
NC_000002.11:g.204721593C>T , CM000664.1:g.204721593C>T GRCh37
NC_000002.10:g.204429838C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2794C>T ENSP00000512655.1:n.47+2794C>T
XR_923797.1:n.225-5603C>T
Search 100 bp 5'
Search 100 bp 3'