Canonical Allele Identifier: CA3405840
Gene: IL13 HGNC NCBI
COSMIC:
COSN26464916 (not active)
COSN26676314 (not active)
MyVariant.info:
GRCh38 chr5:g.132660151T>C
GRCh37 chr5:g.131995843T>C
gnomAD v2:
5:131995843 T / C
gnomAD v3:
5:132660151 T / C
gnomAD v4:
chr5-132660151-T-C
Joint Max Group AF 0.80868015 (NFE)
Genomes Max Group AF 0.78808538 (NFE)
Exomes Max Group AF 0.80964113 (NFE)
dbSNP:
1295686
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132660151T>C , CM000667.2:g.132660151T>C GRCh38
NC_000005.9:g.131995843T>C , CM000667.1:g.131995843T>C GRCh37
NC_000005.8:g.132023742T>C NCBI36
NG_012090.1:g.6979T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000304506.7:c.334-24T>C MANE Select ENSP00000304915.3:n.334-24T>C
ENST00000459878.5:n.338-24T>C
ENST00000462480.1:n.1405-24T>C
ENST00000468334.5:n.707-24T>C
ENST00000487267.5:n.505-24T>C
ENST00000617259.2:c.292-24T>C ENSP00000479835.1:n.292-24T>C
NM_002188.2:c.334-24T>C NP_002179.2:n.334-24T>C
NM_001354991.1:c.139-24T>C NP_001341920.1:n.139-24T>C
NM_001354992.1:c.139-24T>C NP_001341921.1:n.139-24T>C
NM_001354993.1:c.139-24T>C NP_001341922.1:n.139-24T>C
NM_002188.3:c.334-24T>C MANE Select NP_002179.2:n.334-24T>C
NM_001354991.2:c.139-24T>C NP_001341920.1:n.139-24T>C
NM_001354992.2:c.139-24T>C NP_001341921.1:n.139-24T>C
NM_001354993.2:c.139-24T>C NP_001341922.1:n.139-24T>C
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