Canonical Allele Identifier: CA10602845
Gene: CTLA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 280759
ClinVar RCV Id: RCV000274542
dbSNP Id: rs886041906
MyVariant Identifiers: chr2:g.204732725G>A (hg19) chr2:g.203868002G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203868002G>A , CM000664.2:g.203868002G>A GRCh38
NC_000002.11:g.204732725G>A , CM000664.1:g.204732725G>A GRCh37
NC_000002.10:g.204440970G>A NCBI36
NG_011502.1:g.5217G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.60G>A ENSP00000512353.1:p.Trp20Ter
ENST00000696479.1:c.132G>A ENSP00000512655.1:p.Trp44Ter
ENST00000648405.2:c.60G>A MANE Select ENSP00000497102.1:p.Trp20Ter
ENST00000295854.10:c.60G>A ENSP00000295854.6:p.Trp20Ter
ENST00000302823.7:c.60G>A ENSP00000303939.3:p.Trp20Ter
ENST00000472206.1:c.60G>A ENSP00000417779.1:p.Trp20Ter
ENST00000487393.1:n.60G>A
NM_001037631.2:c.60G>A NP_001032720.1:p.Trp20Ter
NM_005214.4:c.60G>A NP_005205.2:p.Trp20Ter
XR_241294.1:n.200G>A
NM_001037631.3:c.60G>A NP_001032720.1:p.Trp20Ter
NM_005214.5:c.60G>A MANE Select NP_005205.2:p.Trp20Ter
Search 100 bp 5'
Search 100 bp 3'