Canonical Allele Identifier: CA1583261761
Gene: IL13 HGNC NCBI

Linked Data

dbSNP Id: rs1752047963
gnomAD v4: 5-132657017-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657017T>C , CM000667.2:g.132657017T>C GRCh38
NC_000005.9:g.131992709T>C , CM000667.1:g.131992709T>C GRCh37
NC_000005.8:g.132020608T>C NCBI36
NG_012090.1:g.3845T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000459878.5:n.107+387T>C
ENST00000468334.5:n.369-49T>C
ENST00000487267.5:n.96-49T>C
NM_001354991.1:c.-93+387T>C NP_001341920.1:n.-93+387T>C
NM_001354992.1:c.-271-49T>C NP_001341921.1:n.-271-49T>C
NM_001354993.1:c.-200-49T>C NP_001341922.1:n.-200-49T>C
NM_001354991.2:c.-93+387T>C NP_001341920.1:n.-93+387T>C
NM_001354992.2:c.-271-49T>C NP_001341921.1:n.-271-49T>C
NM_001354993.2:c.-200-49T>C NP_001341922.1:n.-200-49T>C
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