Canonical Allele Identifier: CA127248737

Gene: IL13

Linked Data

• dbSNP Id: rs534804182
• gnomAD v3: 5-132656944-G-A
• gnomAD v4: 5-132656944-G-A
• MyVariant Identifiers: chr5:g.131992636G>A (hg19) ; chr5:g.132656944G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132656944G>A , CM000667.2:g.132656944G>A	GRCh38
NC_000005.9:g.131992636G>A , CM000667.1:g.131992636G>A	GRCh37
NC_000005.8:g.132020535G>A	NCBI36
NG_012090.1:g.3772G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000459878.5:n.107+314G>A
ENST00000468334.5:n.369-122G>A
ENST00000487267.5:n.96-122G>A
NM_001354991.1:c.-93+314G>A	NP_001341920.1:n.-93+314G>A
NM_001354992.1:c.-271-122G>A	NP_001341921.1:n.-271-122G>A
NM_001354993.1:c.-200-122G>A	NP_001341922.1:n.-200-122G>A
NM_001354991.2:c.-93+314G>A	NP_001341920.1:n.-93+314G>A
NM_001354992.2:c.-271-122G>A	NP_001341921.1:n.-271-122G>A
NM_001354993.2:c.-200-122G>A	NP_001341922.1:n.-200-122G>A