Canonical Allele Identifier: CA2710353815
Gene: IL4 HGNC NCBI

Linked Data

dbSNP Id: rs2149880857

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132679116A>G , CM000667.2:g.132679116A>G GRCh38
NC_000005.9:g.132014808A>G , CM000667.1:g.132014808A>G GRCh37
NC_000005.8:g.132042707A>G NCBI36
NG_023252.1:g.10436A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000231449.7:c.184-598A>G MANE Select ENSP00000231449.2:n.184-598A>G
ENST00000231449.6:c.184-598A>G ENSP00000231449.2:n.184-598A>G
ENST00000350025.2:c.136-598A>G ENSP00000325190.3:n.136-598A>G
ENST00000495905.1:n.150-598A>G
ENST00000622422.1:c.285-598A>G ENSP00000480581.1:n.285-598A>G
NM_000589.3:c.184-598A>G NP_000580.1:n.184-598A>G
NM_172348.2:c.136-598A>G NP_758858.1:n.136-598A>G
NM_001354990.1:c.285-598A>G NP_001341919.1:n.285-598A>G
NR_134248.1:n.1177T>C
NM_000589.4:c.184-598A>G MANE Select NP_000580.1:n.184-598A>G
NM_172348.3:c.136-598A>G NP_758858.1:n.136-598A>G
NM_001354990.2:c.285-598A>G NP_001341919.1:n.285-598A>G