Canonical Allele Identifier: CA1583261729
Gene: IL13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132656944G= , CM000667.2:g.132656944G= GRCh38
NC_000005.9:g.131992636G= , CM000667.1:g.131992636G= GRCh37
NC_000005.8:g.132020535G= NCBI36
NG_012090.1:g.3772G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.107+314G=
ENST00000468334.5:n.369-122G=
ENST00000487267.5:n.96-122G=
NM_001354991.1:c.-93+314G= NP_001341920.1:n.-93+314G=
NM_001354992.1:c.-271-122G= NP_001341921.1:n.-271-122G=
NM_001354993.1:c.-200-122G= NP_001341922.1:n.-200-122G=
NM_001354991.2:c.-93+314G= NP_001341920.1:n.-93+314G=
NM_001354992.2:c.-271-122G= NP_001341921.1:n.-271-122G=
NM_001354993.2:c.-200-122G= NP_001341922.1:n.-200-122G=