Canonical Allele Identifier: CA763579879
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1194074430
MyVariant Identifiers: chr2:g.204722030C>G (hg19) chr2:g.203857307C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857307C>G , CM000664.2:g.203857307C>G GRCh38
NC_000002.11:g.204722030C>G , CM000664.1:g.204722030C>G GRCh37
NC_000002.10:g.204430275C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+3231C>G ENSP00000512655.1:n.47+3231C>G
XR_923797.1:n.225-5166C>G
Search 100 bp 5'
Search 100 bp 3'