Canonical Allele Identifier: CA1583262021
Gene: IL13 HGNC NCBI

Linked Data

dbSNP Id: rs1752062464

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657547_132657548del , CM000667.2:g.132657547_132657548del GRCh38
NC_000005.9:g.131993239_131993240del , CM000667.1:g.131993239_131993240del GRCh37
NC_000005.8:g.132021138_132021139del NCBI36
NG_012090.1:g.4375_4376del

Transcript Alleles

HGVS Amino-acid change
ENST00000459878.5:n.108-743_108-742del
ENST00000468334.5:n.547+303_547+304del
ENST00000487267.5:n.274+303_274+304del
NM_001354991.1:c.-92-743_-92-742del NP_001341920.1:n.-92-743_-92-742del
NM_001354992.1:c.-93+303_-93+304del NP_001341921.1:n.-93+303_-93+304del
NM_001354993.1:c.-22+303_-22+304del NP_001341922.1:n.-22+303_-22+304del
NM_001354991.2:c.-92-743_-92-742del NP_001341920.1:n.-92-743_-92-742del
NM_001354992.2:c.-93+303_-93+304del NP_001341921.1:n.-93+303_-93+304del
NM_001354993.2:c.-22+303_-22+304del NP_001341922.1:n.-22+303_-22+304del