Canonical Allele Identifier: CA1583261766
Gene: IL13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657033T= , CM000667.2:g.132657033T= GRCh38
NC_000005.9:g.131992725T= , CM000667.1:g.131992725T= GRCh37
NC_000005.8:g.132020624T= NCBI36
NG_012090.1:g.3861T=

Transcript Alleles

HGVS Amino-acid change
ENST00000459878.5:n.107+403T=
ENST00000468334.5:n.369-33T=
ENST00000487267.5:n.96-33T=
NM_001354991.1:c.-93+403T= NP_001341920.1:n.-93+403T=
NM_001354992.1:c.-271-33T= NP_001341921.1:n.-271-33T=
NM_001354993.1:c.-200-33T= NP_001341922.1:n.-200-33T=
NM_001354991.2:c.-93+403T= NP_001341920.1:n.-93+403T=
NM_001354992.2:c.-271-33T= NP_001341921.1:n.-271-33T=
NM_001354993.2:c.-200-33T= NP_001341922.1:n.-200-33T=