Canonical Allele Identifier: CA1583272691
Gene: IL4 HGNC NCBI

Linked Data

dbSNP Id: rs2243268

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132678271A>G , CM000667.2:g.132678271A>G GRCh38
NC_000005.9:g.132013963A>G , CM000667.1:g.132013963A>G GRCh37
NC_000005.8:g.132041862A>G NCBI36
NG_023252.1:g.9591A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000231449.7:c.184-1443A>G MANE Select ENSP00000231449.2:n.184-1443A>G
ENST00000231449.6:c.184-1443A>G ENSP00000231449.2:n.184-1443A>G
ENST00000350025.2:c.136-1443A>G ENSP00000325190.3:n.136-1443A>G
ENST00000495905.1:n.150-1443A>G
ENST00000622422.1:c.284+390A>G ENSP00000480581.1:n.284+390A>G
NM_000589.3:c.184-1443A>G NP_000580.1:n.184-1443A>G
NM_172348.2:c.136-1443A>G NP_758858.1:n.136-1443A>G
NM_001354990.1:c.284+390A>G NP_001341919.1:n.284+390A>G
NM_000589.4:c.184-1443A>G MANE Select NP_000580.1:n.184-1443A>G
NM_172348.3:c.136-1443A>G NP_758858.1:n.136-1443A>G
NM_001354990.2:c.284+390A>G NP_001341919.1:n.284+390A>G