Canonical Allele Identifier: CA539148804
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1381878268
gnomAD v2: 2-204732555-A-T
gnomAD v3: 2-203867832-A-T
gnomAD v4: 2-203867832-A-T
MyVariant Identifiers: chr2:g.204732555A>T (hg19) chr2:g.203867832A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867832A>T , CM000664.2:g.203867832A>T GRCh38
NC_000002.11:g.204732555A>T , CM000664.1:g.204732555A>T GRCh37
NC_000002.10:g.204440800A>T NCBI36
NG_011502.1:g.5047A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.-111A>T ENSP00000512353.1:n.-111A>T
ENST00000696479.1:c.48-86A>T ENSP00000512655.1:n.48-86A>T
ENST00000648405.2:c.-111A>T MANE Select ENSP00000497102.1:n.-111A>T
ENST00000302823.7:c.-111A>T ENSP00000303939.3:n.-111A>T
NM_001037631.2:c.-111A>T NP_001032720.1:n.-111A>T
NM_005214.4:c.-111A>T NP_005205.2:n.-111A>T
XR_241294.1:n.30A>T
NM_001037631.3:c.-111A>T NP_001032720.1:n.-111A>T
NM_005214.5:c.-111A>T MANE Select NP_005205.2:n.-111A>T
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