Canonical Allele Identifier: CA1583261775
Gene: IL13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657054A= , CM000667.2:g.132657054A= GRCh38
NC_000005.9:g.131992746A= , CM000667.1:g.131992746A= GRCh37
NC_000005.8:g.132020645A= NCBI36
NG_012090.1:g.3882A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.107+424A=
ENST00000468334.5:n.369-12A=
ENST00000487267.5:n.96-12A=
NM_001354991.1:c.-93+424A= NP_001341920.1:n.-93+424A=
NM_001354992.1:c.-271-12A= NP_001341921.1:n.-271-12A=
NM_001354993.1:c.-200-12A= NP_001341922.1:n.-200-12A=
NM_001354991.2:c.-93+424A= NP_001341920.1:n.-93+424A=
NM_001354992.2:c.-271-12A= NP_001341921.1:n.-271-12A=
NM_001354993.2:c.-200-12A= NP_001341922.1:n.-200-12A=