Canonical Allele Identifier: CA1322144075
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1581567818

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203856971C>T , CM000664.2:g.203856971C>T GRCh38
NC_000002.11:g.204721694C>T , CM000664.1:g.204721694C>T GRCh37
NC_000002.10:g.204429939C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696479.1:c.47+2895C>T ENSP00000512655.1:n.47+2895C>T
XR_923797.1:n.225-5502C>T