Canonical Allele Identifier: CA127249290
Gene: IL13 HGNC NCBI

Linked Data

dbSNP Id: rs981809271
gnomAD v2: 5-131993326-A-C
gnomAD v3: 5-132657634-A-C
gnomAD v4: 5-132657634-A-C
MyVariant Identifiers: chr5:g.131993326A>C (hg19) chr5:g.132657634A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657634A>C , CM000667.2:g.132657634A>C GRCh38
NC_000005.9:g.131993326A>C , CM000667.1:g.131993326A>C GRCh37
NC_000005.8:g.132021225A>C NCBI36
NG_012090.1:g.4462A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000459878.5:n.108-656A>C
ENST00000468334.5:n.547+390A>C
ENST00000487267.5:n.274+390A>C
NM_001354991.1:c.-92-656A>C NP_001341920.1:n.-92-656A>C
NM_001354992.1:c.-93+390A>C NP_001341921.1:n.-93+390A>C
NM_001354993.1:c.-22+390A>C NP_001341922.1:n.-22+390A>C
NM_001354991.2:c.-92-656A>C NP_001341920.1:n.-92-656A>C
NM_001354992.2:c.-93+390A>C NP_001341921.1:n.-93+390A>C
NM_001354993.2:c.-22+390A>C NP_001341922.1:n.-22+390A>C
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