Canonical Allele Identifier: CA2580575021
Gene: IL13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657583A>C , CM000667.2:g.132657583A>C GRCh38
NC_000005.9:g.131993275A>C , CM000667.1:g.131993275A>C GRCh37
NC_000005.8:g.132021174A>C NCBI36
NG_012090.1:g.4411A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000459878.5:n.108-707A>C
ENST00000468334.5:n.547+339A>C
ENST00000487267.5:n.274+339A>C
NM_001354991.1:c.-92-707A>C NP_001341920.1:n.-92-707A>C
NM_001354992.1:c.-93+339A>C NP_001341921.1:n.-93+339A>C
NM_001354993.1:c.-22+339A>C NP_001341922.1:n.-22+339A>C
NM_001354991.2:c.-92-707A>C NP_001341920.1:n.-92-707A>C
NM_001354992.2:c.-93+339A>C NP_001341921.1:n.-93+339A>C
NM_001354993.2:c.-22+339A>C NP_001341922.1:n.-22+339A>C