Canonical Allele Identifier: CA360944393

Gene: IL13

Linked Data

• dbSNP Id: rs1337202282
• gnomAD v2: 5-131995967-T-C
• gnomAD v4: 5-132660275-T-C
• MyVariant Identifiers: chr5:g.131995967T>C (hg19) ; chr5:g.132660275T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660275T>C , CM000667.2:g.132660275T>C	GRCh38
NC_000005.9:g.131995967T>C , CM000667.1:g.131995967T>C	GRCh37
NC_000005.8:g.132023866T>C	NCBI36
NG_012090.1:g.7103T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.434T>C MANE Select	ENSP00000304915.3:p.Phe145Ser
ENST00000459878.5:n.438T>C
ENST00000462480.1:n.1505T>C
ENST00000468334.5:n.807T>C
ENST00000487267.5:n.605T>C
ENST00000617259.2:c.392T>C	ENSP00000479835.1:p.Phe131Ser
NM_002188.2:c.434T>C	NP_002179.2:p.Phe145Ser
NM_001354991.1:c.239T>C	NP_001341920.1:p.Phe80Ser
NM_001354992.1:c.239T>C	NP_001341921.1:p.Phe80Ser
NM_001354993.1:c.239T>C	NP_001341922.1:p.Phe80Ser
NM_002188.3:c.434T>C MANE Select	NP_002179.2:p.Phe145Ser
NM_001354991.2:c.239T>C	NP_001341920.1:p.Phe80Ser
NM_001354992.2:c.239T>C	NP_001341921.1:p.Phe80Ser
NM_001354993.2:c.239T>C	NP_001341922.1:p.Phe80Ser