Canonical Allele Identifier: CA1583262017
Gene: IL13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657542G= , CM000667.2:g.132657542G= GRCh38
NC_000005.9:g.131993234G= , CM000667.1:g.131993234G= GRCh37
NC_000005.8:g.132021133G= NCBI36
NG_012090.1:g.4370G=

Transcript Alleles

HGVS Amino-acid change
ENST00000459878.5:n.108-748G=
ENST00000468334.5:n.547+298G=
ENST00000487267.5:n.274+298G=
NM_001354991.1:c.-92-748G= NP_001341920.1:n.-92-748G=
NM_001354992.1:c.-93+298G= NP_001341921.1:n.-93+298G=
NM_001354993.1:c.-22+298G= NP_001341922.1:n.-22+298G=
NM_001354991.2:c.-92-748G= NP_001341920.1:n.-92-748G=
NM_001354992.2:c.-93+298G= NP_001341921.1:n.-93+298G=
NM_001354993.2:c.-22+298G= NP_001341922.1:n.-22+298G=