Canonical Allele Identifier: CA127249241

Gene: IL13

Linked Data

• dbSNP Id: rs886279006
• MyVariant Identifiers: chr5:g.131993232A>C (hg19) ; chr5:g.132657540A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132657540A>C , CM000667.2:g.132657540A>C	GRCh38
NC_000005.9:g.131993232A>C , CM000667.1:g.131993232A>C	GRCh37
NC_000005.8:g.132021131A>C	NCBI36
NG_012090.1:g.4368A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000459878.5:n.108-750A>C
ENST00000468334.5:n.547+296A>C
ENST00000487267.5:n.274+296A>C
NM_001354991.1:c.-92-750A>C	NP_001341920.1:n.-92-750A>C
NM_001354992.1:c.-93+296A>C	NP_001341921.1:n.-93+296A>C
NM_001354993.1:c.-22+296A>C	NP_001341922.1:n.-22+296A>C
NM_001354991.2:c.-92-750A>C	NP_001341920.1:n.-92-750A>C
NM_001354992.2:c.-93+296A>C	NP_001341921.1:n.-93+296A>C
NM_001354993.2:c.-22+296A>C	NP_001341922.1:n.-22+296A>C