Canonical Allele Identifier: CA1322147897
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1581570838

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866293G>C , CM000664.2:g.203866293G>C GRCh38
NC_000002.11:g.204731016G>C , CM000664.1:g.204731016G>C GRCh37
NC_000002.10:g.204439261G>C NCBI36
NG_011502.1:g.3508G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.48-1625G>C ENSP00000512655.1:n.48-1625G>C