Canonical Allele Identifier: CA804022920
Gene: IL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132678417A>T , CM000667.2:g.132678417A>T GRCh38
NC_000005.9:g.132014109A>T , CM000667.1:g.132014109A>T GRCh37
NC_000005.8:g.132042008A>T NCBI36
NG_023252.1:g.9737A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231449.7:c.184-1297A>T MANE Select ENSP00000231449.2:n.184-1297A>T
ENST00000231449.6:c.184-1297A>T ENSP00000231449.2:n.184-1297A>T
ENST00000350025.2:c.136-1297A>T ENSP00000325190.3:n.136-1297A>T
ENST00000495905.1:n.150-1297A>T
ENST00000622422.1:c.284+536A>T ENSP00000480581.1:n.284+536A>T
NM_000589.3:c.184-1297A>T NP_000580.1:n.184-1297A>T
NM_172348.2:c.136-1297A>T NP_758858.1:n.136-1297A>T
NM_001354990.1:c.284+536A>T NP_001341919.1:n.284+536A>T
NM_000589.4:c.184-1297A>T MANE Select NP_000580.1:n.184-1297A>T
NM_172348.3:c.136-1297A>T NP_758858.1:n.136-1297A>T
NM_001354990.2:c.284+536A>T NP_001341919.1:n.284+536A>T