Canonical Allele Identifier: CA1583262032
Gene: IL13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657569G= , CM000667.2:g.132657569G= GRCh38
NC_000005.9:g.131993261G= , CM000667.1:g.131993261G= GRCh37
NC_000005.8:g.132021160G= NCBI36
NG_012090.1:g.4397G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.108-721G=
ENST00000468334.5:n.547+325G=
ENST00000487267.5:n.274+325G=
NM_001354991.1:c.-92-721G= NP_001341920.1:n.-92-721G=
NM_001354992.1:c.-93+325G= NP_001341921.1:n.-93+325G=
NM_001354993.1:c.-22+325G= NP_001341922.1:n.-22+325G=
NM_001354991.2:c.-92-721G= NP_001341920.1:n.-92-721G=
NM_001354992.2:c.-93+325G= NP_001341921.1:n.-93+325G=
NM_001354993.2:c.-22+325G= NP_001341922.1:n.-22+325G=
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