Canonical Allele Identifier: CA12074133
Gene: IL4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132678097G>A , CM000667.2:g.132678097G>A GRCh38
NC_000005.9:g.132013789G>A , CM000667.1:g.132013789G>A GRCh37
NC_000005.8:g.132041688G>A NCBI36
NG_023252.1:g.9417G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231449.7:c.184-1617G>A MANE Select ENSP00000231449.2:n.184-1617G>A
ENST00000231449.6:c.184-1617G>A ENSP00000231449.2:n.184-1617G>A
ENST00000350025.2:c.136-1617G>A ENSP00000325190.3:n.136-1617G>A
ENST00000495905.1:n.150-1617G>A
ENST00000622422.1:c.284+216G>A ENSP00000480581.1:n.284+216G>A
NM_000589.3:c.184-1617G>A NP_000580.1:n.184-1617G>A
NM_172348.2:c.136-1617G>A NP_758858.1:n.136-1617G>A
NM_001354990.1:c.284+216G>A NP_001341919.1:n.284+216G>A
NM_000589.4:c.184-1617G>A MANE Select NP_000580.1:n.184-1617G>A
NM_172348.3:c.136-1617G>A NP_758858.1:n.136-1617G>A
NM_001354990.2:c.284+216G>A NP_001341919.1:n.284+216G>A
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