Canonical Allele Identifier: CA1583277044
Gene: IL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132682440A>C , CM000667.2:g.132682440A>C GRCh38
NC_000005.9:g.132018132A>C , CM000667.1:g.132018132A>C GRCh37
NC_000005.8:g.132046031A>C NCBI36
NG_023252.1:g.13760A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231449.7:c.361-46A>C MANE Select ENSP00000231449.2:n.361-46A>C
ENST00000231449.6:c.361-46A>C ENSP00000231449.2:n.361-46A>C
ENST00000350025.2:c.313-46A>C ENSP00000325190.3:n.313-46A>C
ENST00000622422.1:c.*51-46A>C ENSP00000480581.1:n.*51-46A>C
NM_000589.3:c.361-46A>C NP_000580.1:n.361-46A>C
NM_172348.2:c.313-46A>C NP_758858.1:n.313-46A>C
XR_948791.1:n.176+14T>G
NM_001354990.1:c.*51-46A>C NP_001341919.1:n.*51-46A>C
NR_134248.1:n.176+14T>G
NM_000589.4:c.361-46A>C MANE Select NP_000580.1:n.361-46A>C
NM_172348.3:c.313-46A>C NP_758858.1:n.313-46A>C
NM_001354990.2:c.*51-46A>C NP_001341919.1:n.*51-46A>C