Canonical Allele Identifier: CA494470563

Gene: IL4R

Linked Data

• dbSNP Id: rs1596546050
• MyVariant Identifiers: chr16:g.27374041A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362720A>C , CM000678.2:g.27362720A>C	GRCh38
NC_000016.9:g.27374041A>C , CM000678.1:g.27374041A>C	GRCh37
NC_000016.8:g.27281542A>C	NCBI36
NG_012086.1:g.53791A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1368A>C MANE Select	ENSP00000379111.2:p.Ala456=
ENST00000170630.6:c.1323A>C	ENSP00000170630.3:p.Ala441=
ENST00000395762.6:c.1368A>C	ENSP00000379111.2:p.Ala456=
ENST00000543915.6:c.1368A>C	ENSP00000441667.2:p.Ala456=
ENST00000565352.1:c.230-1383A>C	ENSP00000461268.1:n.230-1383A>C
ENST00000568746.5:c.*1411A>C	ENSP00000455714.1:n.*1411A>C
NM_000418.3:c.1368A>C	NP_000409.1:p.Ala456=
NM_001257406.1:c.1368A>C	NP_001244335.1:p.Ala456=
NM_001257407.1:c.1323A>C	NP_001244336.1:p.Ala441=
NM_001257997.1:c.888A>C	NP_001244926.1:p.Ala296=
XM_005255308.2:c.477A>C	XP_005255365.1:p.Ala159=
XM_006721043.1:c.417A>C	XP_006721106.1:p.Ala139=
XM_011545825.1:c.1368A>C	XP_011544127.1:p.Ala456=
XM_011545826.1:c.1368A>C	XP_011544128.1:p.Ala456=
XM_011545827.1:c.1368A>C	XP_011544129.1:p.Ala456=
XM_011545828.1:c.1101A>C	XP_011544130.1:p.Ala367=
XM_011545829.1:c.1071A>C	XP_011544131.1:p.Ala357=
XM_011545830.1:c.1071A>C	XP_011544132.1:p.Ala357=
XM_011545831.1:c.1071A>C	XP_011544133.1:p.Ala357=
XM_011545832.1:c.1071A>C	XP_011544134.1:p.Ala357=
XM_011545833.1:c.1071A>C	XP_011544135.1:p.Ala357=
XM_011545834.1:c.945A>C	XP_011544136.1:p.Ala315=
XM_011545826.2:c.1368A>C	XP_011544128.1:p.Ala456=
XM_011545827.2:c.1368A>C	XP_011544129.1:p.Ala456=
XM_011545828.2:c.1101A>C	XP_011544130.1:p.Ala367=
XM_011545830.2:c.1071A>C	XP_011544132.1:p.Ala357=
XM_011545833.2:c.1071A>C	XP_011544135.1:p.Ala357=
XM_011545834.2:c.945A>C	XP_011544136.1:p.Ala315=
XM_017023211.1:c.*403A>C	XP_016878700.1:n.*403A>C
NM_000418.4:c.1368A>C MANE Select	NP_000409.1:p.Ala456=
NM_001257406.2:c.1368A>C	NP_001244335.1:p.Ala456=
NM_001257407.2:c.1323A>C	NP_001244336.1:p.Ala441=
NM_001257997.2:c.888A>C	NP_001244926.1:p.Ala296=