Canonical Allele Identifier: CA2675221220
Gene: IL13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132656960G>T , CM000667.2:g.132656960G>T GRCh38
NC_000005.9:g.131992652G>T , CM000667.1:g.131992652G>T GRCh37
NC_000005.8:g.132020551G>T NCBI36
NG_012090.1:g.3788G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.107+330G>T
ENST00000468334.5:n.369-106G>T
ENST00000487267.5:n.96-106G>T
NM_001354991.1:c.-93+330G>T NP_001341920.1:n.-93+330G>T
NM_001354992.1:c.-271-106G>T NP_001341921.1:n.-271-106G>T
NM_001354993.1:c.-200-106G>T NP_001341922.1:n.-200-106G>T
NM_001354991.2:c.-93+330G>T NP_001341920.1:n.-93+330G>T
NM_001354992.2:c.-271-106G>T NP_001341921.1:n.-271-106G>T
NM_001354993.2:c.-200-106G>T NP_001341922.1:n.-200-106G>T