Canonical Allele Identifier: CA127248819

Gene: IL13

Linked Data

• dbSNP Id: rs577463465
• gnomAD v2: 5-131992721-T-C
• gnomAD v3: 5-132657029-T-C
• gnomAD v4: 5-132657029-T-C
• MyVariant Identifiers: chr5:g.131992721T>C (hg19) ; chr5:g.132657029T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132657029T>C , CM000667.2:g.132657029T>C	GRCh38
NC_000005.9:g.131992721T>C , CM000667.1:g.131992721T>C	GRCh37
NC_000005.8:g.132020620T>C	NCBI36
NG_012090.1:g.3857T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000459878.5:n.107+399T>C
ENST00000468334.5:n.369-37T>C
ENST00000487267.5:n.96-37T>C
NM_001354991.1:c.-93+399T>C	NP_001341920.1:n.-93+399T>C
NM_001354992.1:c.-271-37T>C	NP_001341921.1:n.-271-37T>C
NM_001354993.1:c.-200-37T>C	NP_001341922.1:n.-200-37T>C
NM_001354991.2:c.-93+399T>C	NP_001341920.1:n.-93+399T>C
NM_001354992.2:c.-271-37T>C	NP_001341921.1:n.-271-37T>C
NM_001354993.2:c.-200-37T>C	NP_001341922.1:n.-200-37T>C