Canonical Allele Identifier: CA127248804

Gene: IL13

Linked Data

• dbSNP Id: rs1050580003
• gnomAD v2: 5-131992710-C-G
• gnomAD v3: 5-132657018-C-G
• gnomAD v4: 5-132657018-C-G
• MyVariant Identifiers: chr5:g.131992710C>G (hg19) ; chr5:g.132657018C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132657018C>G , CM000667.2:g.132657018C>G	GRCh38
NC_000005.9:g.131992710C>G , CM000667.1:g.131992710C>G	GRCh37
NC_000005.8:g.132020609C>G	NCBI36
NG_012090.1:g.3846C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000459878.5:n.107+388C>G
ENST00000468334.5:n.369-48C>G
ENST00000487267.5:n.96-48C>G
NM_001354991.1:c.-93+388C>G	NP_001341920.1:n.-93+388C>G
NM_001354992.1:c.-271-48C>G	NP_001341921.1:n.-271-48C>G
NM_001354993.1:c.-200-48C>G	NP_001341922.1:n.-200-48C>G
NM_001354991.2:c.-93+388C>G	NP_001341920.1:n.-93+388C>G
NM_001354992.2:c.-271-48C>G	NP_001341921.1:n.-271-48C>G
NM_001354993.2:c.-200-48C>G	NP_001341922.1:n.-200-48C>G