Canonical Allele Identifier: CA1583270934

Gene: IL4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132677033T= , CM000667.2:g.132677033T=	GRCh38
NC_000005.9:g.132012725T= , CM000667.1:g.132012725T=	GRCh37
NC_000005.8:g.132040624T=	NCBI36
NG_023252.1:g.8353T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000589.4:c.183+2527T= MANE Select	NP_000580.1:n.183+2527T=
ENST00000231449.7:c.183+2527T= MANE Select	ENSP00000231449.2:n.183+2527T=
NM_000589.3:c.183+2527T=	NP_000580.1:n.183+2527T=
NM_001354990.1:c.184-748T=	NP_001341919.1:n.184-748T=
NM_001354990.2:c.184-748T=	NP_001341919.1:n.184-748T=
NM_172348.2:c.136-2681T=	NP_758858.1:n.136-2681T=
NM_172348.3:c.136-2681T=	NP_758858.1:n.136-2681T=
ENST00000231449.6:c.183+2527T=	ENSP00000231449.2:n.183+2527T=
ENST00000350025.2:c.136-2681T=	ENSP00000325190.3:n.136-2681T=
ENST00000495905.1:n.149+2527T=
ENST00000622422.1:c.184-748T=	ENSP00000480581.1:n.184-748T=