Canonical Allele Identifier: CA1583277060
Gene: IL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132682477C= , CM000667.2:g.132682477C= GRCh38
NC_000005.9:g.132018169C= , CM000667.1:g.132018169C= GRCh37
NC_000005.8:g.132046068C= NCBI36
NG_023252.1:g.13797C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231449.7:c.361-9C= MANE Select ENSP00000231449.2:n.361-9C=
ENST00000231449.6:c.361-9C= ENSP00000231449.2:n.361-9C=
ENST00000350025.2:c.313-9C= ENSP00000325190.3:n.313-9C=
ENST00000622422.1:c.*51-9C= ENSP00000480581.1:n.*51-9C=
NM_000589.3:c.361-9C= NP_000580.1:n.361-9C=
NM_172348.2:c.313-9C= NP_758858.1:n.313-9C=
XR_948791.1:n.153G=
NM_001354990.1:c.*51-9C= NP_001341919.1:n.*51-9C=
NR_134248.1:n.153G=
NM_000589.4:c.361-9C= MANE Select NP_000580.1:n.361-9C=
NM_172348.3:c.313-9C= NP_758858.1:n.313-9C=
NM_001354990.2:c.*51-9C= NP_001341919.1:n.*51-9C=