Canonical Allele Identifier: CA3405864

Gene: IL13

Linked Data

• dbSNP Id: rs761274909
• ExAC: 5:131995969 A / G
• gnomAD v2: 5-131995969-A-G
• MyVariant Identifiers: chr5:g.131995969A>G (hg19) ; chr5:g.132660277A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660277A>G , CM000667.2:g.132660277A>G	GRCh38
NC_000005.9:g.131995969A>G , CM000667.1:g.131995969A>G	GRCh37
NC_000005.8:g.132023868A>G	NCBI36
NG_012090.1:g.7105A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000304506.7:c.436A>G MANE Select	ENSP00000304915.3:p.Asn146Asp
ENST00000459878.5:n.440A>G
ENST00000462480.1:n.1507A>G
ENST00000468334.5:n.809A>G
ENST00000487267.5:n.607A>G
ENST00000617259.2:c.394A>G	ENSP00000479835.1:p.Asn132Asp
NM_002188.2:c.436A>G	NP_002179.2:p.Asn146Asp
NM_001354991.1:c.241A>G	NP_001341920.1:p.Asn81Asp
NM_001354992.1:c.241A>G	NP_001341921.1:p.Asn81Asp
NM_001354993.1:c.241A>G	NP_001341922.1:p.Asn81Asp
NM_002188.3:c.436A>G MANE Select	NP_002179.2:p.Asn146Asp
NM_001354991.2:c.241A>G	NP_001341920.1:p.Asn81Asp
NM_001354992.2:c.241A>G	NP_001341921.1:p.Asn81Asp
NM_001354993.2:c.241A>G	NP_001341922.1:p.Asn81Asp