Canonical Allele Identifier: CA2675221378
Gene: IL13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657043A>G , CM000667.2:g.132657043A>G GRCh38
NC_000005.9:g.131992735A>G , CM000667.1:g.131992735A>G GRCh37
NC_000005.8:g.132020634A>G NCBI36
NG_012090.1:g.3871A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.107+413A>G
ENST00000468334.5:n.369-23A>G
ENST00000487267.5:n.96-23A>G
NM_001354991.1:c.-93+413A>G NP_001341920.1:n.-93+413A>G
NM_001354992.1:c.-271-23A>G NP_001341921.1:n.-271-23A>G
NM_001354993.1:c.-200-23A>G NP_001341922.1:n.-200-23A>G
NM_001354991.2:c.-93+413A>G NP_001341920.1:n.-93+413A>G
NM_001354992.2:c.-271-23A>G NP_001341921.1:n.-271-23A>G
NM_001354993.2:c.-200-23A>G NP_001341922.1:n.-200-23A>G