Canonical Allele Identifier: CA3406000
Gene: IL4 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.132682477C>A
GRCh37 chr5:g.132018169C>A
gnomAD v2:
5:132018169 C / A
gnomAD v3:
5:132682477 C / A
gnomAD v4:
chr5-132682477-C-A
Joint Max Group AF 0.73670197 (EAS)
Genomes Max Group AF 0.75557941 (EAS)
Exomes Max Group AF 0.73205816 (EAS)
dbSNP:
2243290
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Genomic Alleles

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

Transcript Alleles

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