Canonical Allele Identifier: CA1583272500
Gene: IL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132678194G= , CM000667.2:g.132678194G= GRCh38
NC_000005.9:g.132013886G= , CM000667.1:g.132013886G= GRCh37
NC_000005.8:g.132041785G= NCBI36
NG_023252.1:g.9514G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231449.7:c.184-1520G= MANE Select ENSP00000231449.2:n.184-1520G=
ENST00000231449.6:c.184-1520G= ENSP00000231449.2:n.184-1520G=
ENST00000350025.2:c.136-1520G= ENSP00000325190.3:n.136-1520G=
ENST00000495905.1:n.150-1520G=
ENST00000622422.1:c.284+313G= ENSP00000480581.1:n.284+313G=
NM_000589.3:c.184-1520G= NP_000580.1:n.184-1520G=
NM_172348.2:c.136-1520G= NP_758858.1:n.136-1520G=
NM_001354990.1:c.284+313G= NP_001341919.1:n.284+313G=
NM_000589.4:c.184-1520G= MANE Select NP_000580.1:n.184-1520G=
NM_172348.3:c.136-1520G= NP_758858.1:n.136-1520G=
NM_001354990.2:c.284+313G= NP_001341919.1:n.284+313G=