Canonical Allele Identifier: CA2675221188

Gene: IL13

Linked Data

• gnomAD v4: 5-132656936-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132656936C>T , CM000667.2:g.132656936C>T	GRCh38
NC_000005.9:g.131992628C>T , CM000667.1:g.131992628C>T	GRCh37
NC_000005.8:g.132020527C>T	NCBI36
NG_012090.1:g.3764C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000459878.5:n.107+306C>T
ENST00000468334.5:n.369-130C>T
ENST00000487267.5:n.96-130C>T
NM_001354991.1:c.-93+306C>T	NP_001341920.1:n.-93+306C>T
NM_001354992.1:c.-271-130C>T	NP_001341921.1:n.-271-130C>T
NM_001354993.1:c.-200-130C>T	NP_001341922.1:n.-200-130C>T
NM_001354991.2:c.-93+306C>T	NP_001341920.1:n.-93+306C>T
NM_001354992.2:c.-271-130C>T	NP_001341921.1:n.-271-130C>T
NM_001354993.2:c.-200-130C>T	NP_001341922.1:n.-200-130C>T