Canonical Allele Identifier: CA2662768238
Gene: CTLA4 HGNC NCBI

Linked Data

gnomAD v4: 2-203867921-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867921T>C , CM000664.2:g.203867921T>C GRCh38
NC_000002.11:g.204732644T>C , CM000664.1:g.204732644T>C GRCh37
NC_000002.10:g.204440889T>C NCBI36
NG_011502.1:g.5136T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.-22T>C ENSP00000512353.1:n.-22T>C
ENST00000696479.1:c.51T>C ENSP00000512655.1:p.Pro17=
ENST00000648405.2:c.-22T>C MANE Select ENSP00000497102.1:n.-22T>C
ENST00000302823.7:c.-22T>C ENSP00000303939.3:n.-22T>C
NM_001037631.2:c.-22T>C NP_001032720.1:n.-22T>C
NM_005214.4:c.-22T>C NP_005205.2:n.-22T>C
XR_241294.1:n.119T>C
NM_001037631.3:c.-22T>C NP_001032720.1:n.-22T>C
NM_005214.5:c.-22T>C MANE Select NP_005205.2:n.-22T>C
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