Canonical Allele Identifier: CA2710354360
Gene: IL13 HGNC NCBI

Linked Data

dbSNP Id: rs2149873646
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657611T>A , CM000667.2:g.132657611T>A GRCh38
NC_000005.9:g.131993303T>A , CM000667.1:g.131993303T>A GRCh37
NC_000005.8:g.132021202T>A NCBI36
NG_012090.1:g.4439T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000459878.5:n.108-679T>A
ENST00000468334.5:n.547+367T>A
ENST00000487267.5:n.274+367T>A
NM_001354991.1:c.-92-679T>A NP_001341920.1:n.-92-679T>A
NM_001354992.1:c.-93+367T>A NP_001341921.1:n.-93+367T>A
NM_001354993.1:c.-22+367T>A NP_001341922.1:n.-22+367T>A
NM_001354991.2:c.-92-679T>A NP_001341920.1:n.-92-679T>A
NM_001354992.2:c.-93+367T>A NP_001341921.1:n.-93+367T>A
NM_001354993.2:c.-22+367T>A NP_001341922.1:n.-22+367T>A
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