Canonical Allele Identifier: CA1322148558
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688655944
gnomAD v4: 2-203867906-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867906T>G , CM000664.2:g.203867906T>G GRCh38
NC_000002.11:g.204732629T>G , CM000664.1:g.204732629T>G GRCh37
NC_000002.10:g.204440874T>G NCBI36
NG_011502.1:g.5121T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.-37T>G ENSP00000512353.1:n.-37T>G
ENST00000696479.1:c.48-12T>G ENSP00000512655.1:n.48-12T>G
ENST00000648405.2:c.-37T>G MANE Select ENSP00000497102.1:n.-37T>G
ENST00000302823.7:c.-37T>G ENSP00000303939.3:n.-37T>G
NM_001037631.2:c.-37T>G NP_001032720.1:n.-37T>G
NM_005214.4:c.-37T>G NP_005205.2:n.-37T>G
XR_241294.1:n.104T>G
NM_001037631.3:c.-37T>G NP_001032720.1:n.-37T>G
NM_005214.5:c.-37T>G MANE Select NP_005205.2:n.-37T>G
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