Canonical Allele Identifier: CA2701403218
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs2105767307

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203857360T>C , CM000664.2:g.203857360T>C GRCh38
NC_000002.11:g.204722083T>C , CM000664.1:g.204722083T>C GRCh37
NC_000002.10:g.204430328T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.47+3284T>C ENSP00000512655.1:n.47+3284T>C
XR_923797.1:n.225-5113T>C