Canonical Allele Identifier: CA1583261994
Gene: IL13 HGNC NCBI

Linked Data

dbSNP Id: rs564856494
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657508_132657517del , CM000667.2:g.132657508_132657517del GRCh38
NC_000005.9:g.131993200_131993209del , CM000667.1:g.131993200_131993209del GRCh37
NC_000005.8:g.132021099_132021108del NCBI36
NG_012090.1:g.4336_4345del

Transcript Alleles

HGVS Amino-acid change
ENST00000459878.5:n.108-782_108-773del
ENST00000468334.5:n.547+264_547+273del
ENST00000487267.5:n.274+264_274+273del
NM_001354991.1:c.-92-782_-92-773del NP_001341920.1:n.-92-782_-92-773del
NM_001354992.1:c.-93+264_-93+273del NP_001341921.1:n.-93+264_-93+273del
NM_001354993.1:c.-22+264_-22+273del NP_001341922.1:n.-22+264_-22+273del
NM_001354991.2:c.-92-782_-92-773del NP_001341920.1:n.-92-782_-92-773del
NM_001354992.2:c.-93+264_-93+273del NP_001341921.1:n.-93+264_-93+273del
NM_001354993.2:c.-22+264_-22+273del NP_001341922.1:n.-22+264_-22+273del
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