Canonical Allele Identifier: CA804011356

Gene: IL13

Linked Data

• dbSNP Id: rs1447232989
• gnomAD v3: 5-132657602-C-T
• gnomAD v4: 5-132657602-C-T
• MyVariant Identifiers: chr5:g.131993294C>T (hg19) ; chr5:g.132657602C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132657602C>T , CM000667.2:g.132657602C>T	GRCh38
NC_000005.9:g.131993294C>T , CM000667.1:g.131993294C>T	GRCh37
NC_000005.8:g.132021193C>T	NCBI36
NG_012090.1:g.4430C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000459878.5:n.108-688C>T
ENST00000468334.5:n.547+358C>T
ENST00000487267.5:n.274+358C>T
NM_001354991.1:c.-92-688C>T	NP_001341920.1:n.-92-688C>T
NM_001354992.1:c.-93+358C>T	NP_001341921.1:n.-93+358C>T
NM_001354993.1:c.-22+358C>T	NP_001341922.1:n.-22+358C>T
NM_001354991.2:c.-92-688C>T	NP_001341920.1:n.-92-688C>T
NM_001354992.2:c.-93+358C>T	NP_001341921.1:n.-93+358C>T
NM_001354993.2:c.-22+358C>T	NP_001341922.1:n.-22+358C>T