Canonical Allele Identifier: CA127248831
Gene: IL13 HGNC NCBI

Linked Data

dbSNP Id: rs938280905
gnomAD v4: 5-132657037-G-A
MyVariant Identifiers: chr5:g.131992729G>A (hg19) chr5:g.132657037G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657037G>A , CM000667.2:g.132657037G>A GRCh38
NC_000005.9:g.131992729G>A , CM000667.1:g.131992729G>A GRCh37
NC_000005.8:g.132020628G>A NCBI36
NG_012090.1:g.3865G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000459878.5:n.107+407G>A
ENST00000468334.5:n.369-29G>A
ENST00000487267.5:n.96-29G>A
NM_001354991.1:c.-93+407G>A NP_001341920.1:n.-93+407G>A
NM_001354992.1:c.-271-29G>A NP_001341921.1:n.-271-29G>A
NM_001354993.1:c.-200-29G>A NP_001341922.1:n.-200-29G>A
NM_001354991.2:c.-93+407G>A NP_001341920.1:n.-93+407G>A
NM_001354992.2:c.-271-29G>A NP_001341921.1:n.-271-29G>A
NM_001354993.2:c.-200-29G>A NP_001341922.1:n.-200-29G>A
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