Canonical Allele Identifier: CA562774077

Gene: IL13

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660151T>A , CM000667.2:g.132660151T>A	GRCh38
NC_000005.9:g.131995843T>A , CM000667.1:g.131995843T>A	GRCh37
NC_000005.8:g.132023742T>A	NCBI36
NG_012090.1:g.6979T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.334-24T>A MANE Select	ENSP00000304915.3:n.334-24T>A
ENST00000459878.5:n.338-24T>A
ENST00000462480.1:n.1405-24T>A
ENST00000468334.5:n.707-24T>A
ENST00000487267.5:n.505-24T>A
ENST00000617259.2:c.292-24T>A	ENSP00000479835.1:n.292-24T>A
NM_002188.2:c.334-24T>A	NP_002179.2:n.334-24T>A
NM_001354991.1:c.139-24T>A	NP_001341920.1:n.139-24T>A
NM_001354992.1:c.139-24T>A	NP_001341921.1:n.139-24T>A
NM_001354993.1:c.139-24T>A	NP_001341922.1:n.139-24T>A
NM_002188.3:c.334-24T>A MANE Select	NP_002179.2:n.334-24T>A
NM_001354991.2:c.139-24T>A	NP_001341920.1:n.139-24T>A
NM_001354992.2:c.139-24T>A	NP_001341921.1:n.139-24T>A
NM_001354993.2:c.139-24T>A	NP_001341922.1:n.139-24T>A