Canonical Allele Identifier: CA1583262013
Gene: IL13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657527A= , CM000667.2:g.132657527A= GRCh38
NC_000005.9:g.131993219A= , CM000667.1:g.131993219A= GRCh37
NC_000005.8:g.132021118A= NCBI36
NG_012090.1:g.4355A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.108-763A=
ENST00000468334.5:n.547+283A=
ENST00000487267.5:n.274+283A=
NM_001354991.1:c.-92-763A= NP_001341920.1:n.-92-763A=
NM_001354992.1:c.-93+283A= NP_001341921.1:n.-93+283A=
NM_001354993.1:c.-22+283A= NP_001341922.1:n.-22+283A=
NM_001354991.2:c.-92-763A= NP_001341920.1:n.-92-763A=
NM_001354992.2:c.-93+283A= NP_001341921.1:n.-93+283A=
NM_001354993.2:c.-22+283A= NP_001341922.1:n.-22+283A=
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