Canonical Allele Identifier: CA1583262033
Gene: IL13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657572G= , CM000667.2:g.132657572G= GRCh38
NC_000005.9:g.131993264G= , CM000667.1:g.131993264G= GRCh37
NC_000005.8:g.132021163G= NCBI36
NG_012090.1:g.4400G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.108-718G=
ENST00000468334.5:n.547+328G=
ENST00000487267.5:n.274+328G=
NM_001354991.1:c.-92-718G= NP_001341920.1:n.-92-718G=
NM_001354992.1:c.-93+328G= NP_001341921.1:n.-93+328G=
NM_001354993.1:c.-22+328G= NP_001341922.1:n.-22+328G=
NM_001354991.2:c.-92-718G= NP_001341920.1:n.-92-718G=
NM_001354992.2:c.-93+328G= NP_001341921.1:n.-93+328G=
NM_001354993.2:c.-22+328G= NP_001341922.1:n.-22+328G=