Canonical Allele Identifier: CA1081664750

Gene: IL4

Linked Data

• dbSNP Id: rs1384825973
• gnomAD v3: 5-132679110-C-T
• gnomAD v4: 5-132679110-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132679110C>T , CM000667.2:g.132679110C>T	GRCh38
NC_000005.9:g.132014802C>T , CM000667.1:g.132014802C>T	GRCh37
NC_000005.8:g.132042701C>T	NCBI36
NG_023252.1:g.10430C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231449.7:c.184-604C>T MANE Select	ENSP00000231449.2:n.184-604C>T
ENST00000231449.6:c.184-604C>T	ENSP00000231449.2:n.184-604C>T
ENST00000350025.2:c.136-604C>T	ENSP00000325190.3:n.136-604C>T
ENST00000495905.1:n.150-604C>T
ENST00000622422.1:c.285-604C>T	ENSP00000480581.1:n.285-604C>T
NM_000589.3:c.184-604C>T	NP_000580.1:n.184-604C>T
NM_172348.2:c.136-604C>T	NP_758858.1:n.136-604C>T
NM_001354990.1:c.285-604C>T	NP_001341919.1:n.285-604C>T
NR_134248.1:n.1183G>A
NM_000589.4:c.184-604C>T MANE Select	NP_000580.1:n.184-604C>T
NM_172348.3:c.136-604C>T	NP_758858.1:n.136-604C>T
NM_001354990.2:c.285-604C>T	NP_001341919.1:n.285-604C>T