Canonical Allele Identifier: CA2675221211
Gene: IL13 HGNC NCBI

Linked Data

gnomAD v4: 5-132656954-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132656954C>A , CM000667.2:g.132656954C>A GRCh38
NC_000005.9:g.131992646C>A , CM000667.1:g.131992646C>A GRCh37
NC_000005.8:g.132020545C>A NCBI36
NG_012090.1:g.3782C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.107+324C>A
ENST00000468334.5:n.369-112C>A
ENST00000487267.5:n.96-112C>A
NM_001354991.1:c.-93+324C>A NP_001341920.1:n.-93+324C>A
NM_001354992.1:c.-271-112C>A NP_001341921.1:n.-271-112C>A
NM_001354993.1:c.-200-112C>A NP_001341922.1:n.-200-112C>A
NM_001354991.2:c.-93+324C>A NP_001341920.1:n.-93+324C>A
NM_001354992.2:c.-271-112C>A NP_001341921.1:n.-271-112C>A
NM_001354993.2:c.-200-112C>A NP_001341922.1:n.-200-112C>A
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