Canonical Allele Identifier: CA127249226

Gene: IL13

Linked Data

• dbSNP Id: rs2069742
• gnomAD v2: 5-131993206-A-G
• gnomAD v3: 5-132657514-A-G
• gnomAD v4: 5-132657514-A-G
• MyVariant Identifiers: chr5:g.131993206A>G (hg19) ; chr5:g.132657514A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132657514A>G , CM000667.2:g.132657514A>G	GRCh38
NC_000005.9:g.131993206A>G , CM000667.1:g.131993206A>G	GRCh37
NC_000005.8:g.132021105A>G	NCBI36
NG_012090.1:g.4342A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000459878.5:n.108-776A>G
ENST00000468334.5:n.547+270A>G
ENST00000487267.5:n.274+270A>G
NM_001354991.1:c.-92-776A>G	NP_001341920.1:n.-92-776A>G
NM_001354992.1:c.-93+270A>G	NP_001341921.1:n.-93+270A>G
NM_001354993.1:c.-22+270A>G	NP_001341922.1:n.-22+270A>G
NM_001354991.2:c.-92-776A>G	NP_001341920.1:n.-92-776A>G
NM_001354992.2:c.-93+270A>G	NP_001341921.1:n.-93+270A>G
NM_001354993.2:c.-22+270A>G	NP_001341922.1:n.-22+270A>G