Canonical Allele Identifier: CA2580590967
Gene: IL4 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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