Canonical Allele Identifier: CA11981417
Gene: IL13 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.132656717A>C
GRCh37 chr5:g.131992409A>C
gnomAD v2:
5:131992409 A / C
gnomAD v3:
5:132656717 A / C
gnomAD v4:
chr5-132656717-A-C
Joint Max Group AF 0.23313649 (EAS)
Genomes Max Group AF 0.23329276 (EAS)
Exomes Max Group AF 0.17151012 (NFE)
dbSNP:
1881457
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132656717A>C , CM000667.2:g.132656717A>C GRCh38
NC_000005.9:g.131992409A>C , CM000667.1:g.131992409A>C GRCh37
NC_000005.8:g.132020308A>C NCBI36
NG_012090.1:g.3545A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.107+87A>C
ENST00000468334.5:n.368+87A>C
ENST00000487267.5:n.95+87A>C
NM_001354991.1:c.-93+87A>C NP_001341920.1:n.-93+87A>C
NM_001354992.1:c.-272+87A>C NP_001341921.1:n.-272+87A>C
NM_001354993.1:c.-201+87A>C NP_001341922.1:n.-201+87A>C
NM_001354991.2:c.-93+87A>C NP_001341920.1:n.-93+87A>C
NM_001354992.2:c.-272+87A>C NP_001341921.1:n.-272+87A>C
NM_001354993.2:c.-201+87A>C NP_001341922.1:n.-201+87A>C
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