Canonical Allele Identifier: CA127249228
Gene: IL13 HGNC NCBI

Linked Data

dbSNP Id: rs55912311
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657530del , CM000667.2:g.132657530del GRCh38
NC_000005.9:g.131993222del , CM000667.1:g.131993222del GRCh37
NC_000005.8:g.132021121del NCBI36
NG_012090.1:g.4358del

Transcript Alleles

HGVS Amino-acid change
ENST00000459878.5:n.108-760del
ENST00000468334.5:n.547+286del
ENST00000487267.5:n.274+286del
NM_001354991.1:c.-92-760del NP_001341920.1:n.-92-760del
NM_001354992.1:c.-93+286del NP_001341921.1:n.-93+286del
NM_001354993.1:c.-22+286del NP_001341922.1:n.-22+286del
NM_001354991.2:c.-92-760del NP_001341920.1:n.-92-760del
NM_001354992.2:c.-93+286del NP_001341921.1:n.-93+286del
NM_001354993.2:c.-22+286del NP_001341922.1:n.-22+286del
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