Canonical Allele Identifier: CA1081654686
Gene: IL13 HGNC NCBI

Linked Data

dbSNP Id: rs1752048587

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657048G>T , CM000667.2:g.132657048G>T GRCh38
NC_000005.9:g.131992740G>T , CM000667.1:g.131992740G>T GRCh37
NC_000005.8:g.132020639G>T NCBI36
NG_012090.1:g.3876G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.107+418G>T
ENST00000468334.5:n.369-18G>T
ENST00000487267.5:n.96-18G>T
NM_001354991.1:c.-93+418G>T NP_001341920.1:n.-93+418G>T
NM_001354992.1:c.-271-18G>T NP_001341921.1:n.-271-18G>T
NM_001354993.1:c.-200-18G>T NP_001341922.1:n.-200-18G>T
NM_001354991.2:c.-93+418G>T NP_001341920.1:n.-93+418G>T
NM_001354992.2:c.-271-18G>T NP_001341921.1:n.-271-18G>T
NM_001354993.2:c.-200-18G>T NP_001341922.1:n.-200-18G>T