Canonical Allele Identifier: CA1583262083
Gene: IL13 HGNC NCBI

Linked Data

dbSNP Id: rs1752065191

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657685C>G , CM000667.2:g.132657685C>G GRCh38
NC_000005.9:g.131993377C>G , CM000667.1:g.131993377C>G GRCh37
NC_000005.8:g.132021276C>G NCBI36
NG_012090.1:g.4513C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.108-605C>G
ENST00000468334.5:n.547+441C>G
ENST00000487267.5:n.274+441C>G
NM_001354991.1:c.-92-605C>G NP_001341920.1:n.-92-605C>G
NM_001354992.1:c.-93+441C>G NP_001341921.1:n.-93+441C>G
NM_001354993.1:c.-22+441C>G NP_001341922.1:n.-22+441C>G
NM_001354991.2:c.-92-605C>G NP_001341920.1:n.-92-605C>G
NM_001354992.2:c.-93+441C>G NP_001341921.1:n.-93+441C>G
NM_001354993.2:c.-22+441C>G NP_001341922.1:n.-22+441C>G