Canonical Allele Identifier: CA2067023
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs774909973

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867924A>G , CM000664.2:g.203867924A>G GRCh38
NC_000002.11:g.204732647A>G , CM000664.1:g.204732647A>G GRCh37
NC_000002.10:g.204440892A>G NCBI36
NG_011502.1:g.5139A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.-19A>G ENSP00000512353.1:n.-19A>G
ENST00000696479.1:c.54A>G ENSP00000512655.1:p.Glu18=
ENST00000648405.2:c.-19A>G MANE Select ENSP00000497102.1:n.-19A>G
ENST00000302823.7:c.-19A>G ENSP00000303939.3:n.-19A>G
NM_001037631.2:c.-19A>G NP_001032720.1:n.-19A>G
NM_005214.4:c.-19A>G NP_005205.2:n.-19A>G
XR_241294.1:n.122A>G
NM_001037631.3:c.-19A>G NP_001032720.1:n.-19A>G
NM_005214.5:c.-19A>G MANE Select NP_005205.2:n.-19A>G