Canonical Allele Identifier: CA804011286
Gene: IL13 HGNC NCBI

Linked Data

dbSNP Id: rs1376916346
MyVariant Identifiers: chr5:g.131993213C>A (hg19) chr5:g.132657521C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657521C>A , CM000667.2:g.132657521C>A GRCh38
NC_000005.9:g.131993213C>A , CM000667.1:g.131993213C>A GRCh37
NC_000005.8:g.132021112C>A NCBI36
NG_012090.1:g.4349C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.108-769C>A
ENST00000468334.5:n.547+277C>A
ENST00000487267.5:n.274+277C>A
NM_001354991.1:c.-92-769C>A NP_001341920.1:n.-92-769C>A
NM_001354992.1:c.-93+277C>A NP_001341921.1:n.-93+277C>A
NM_001354993.1:c.-22+277C>A NP_001341922.1:n.-22+277C>A
NM_001354991.2:c.-92-769C>A NP_001341920.1:n.-92-769C>A
NM_001354992.2:c.-93+277C>A NP_001341921.1:n.-93+277C>A
NM_001354993.2:c.-22+277C>A NP_001341922.1:n.-22+277C>A
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