Canonical Allele Identifier: CA763579789
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1206748477
gnomAD v3: 2-203857031-G-C
gnomAD v4: 2-203857031-G-C
MyVariant Identifiers: chr2:g.204721754G>C (hg19) chr2:g.203857031G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857031G>C , CM000664.2:g.203857031G>C GRCh38
NC_000002.11:g.204721754G>C , CM000664.1:g.204721754G>C GRCh37
NC_000002.10:g.204429999G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2955G>C ENSP00000512655.1:n.47+2955G>C
XR_923797.1:n.225-5442G>C
Search 100 bp 5'
Search 100 bp 3'