Canonical Allele Identifier: CA395298813

Gene: IL4R

Linked Data

• MyVariant Identifiers: chr16:g.27374071C>G (hg19) ; chr16:g.27362750C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362750C>G , CM000678.2:g.27362750C>G	GRCh38
NC_000016.9:g.27374071C>G , CM000678.1:g.27374071C>G	GRCh37
NC_000016.8:g.27281572C>G	NCBI36
NG_012086.1:g.53821C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1398C>G MANE Select	ENSP00000379111.2:p.His466Gln
ENST00000170630.6:c.1353C>G	ENSP00000170630.3:p.His451Gln
ENST00000395762.6:c.1398C>G	ENSP00000379111.2:p.His466Gln
ENST00000543915.6:c.1398C>G	ENSP00000441667.2:p.His466Gln
ENST00000565352.1:c.230-1353C>G	ENSP00000461268.1:n.230-1353C>G
ENST00000568746.5:c.*1441C>G	ENSP00000455714.1:n.*1441C>G
NM_000418.3:c.1398C>G	NP_000409.1:p.His466Gln
NM_001257406.1:c.1398C>G	NP_001244335.1:p.His466Gln
NM_001257407.1:c.1353C>G	NP_001244336.1:p.His451Gln
NM_001257997.1:c.918C>G	NP_001244926.1:p.His306Gln
XM_005255308.2:c.507C>G	XP_005255365.1:p.His169Gln
XM_006721043.1:c.447C>G	XP_006721106.1:p.His149Gln
XM_011545825.1:c.1398C>G	XP_011544127.1:p.His466Gln
XM_011545826.1:c.1398C>G	XP_011544128.1:p.His466Gln
XM_011545827.1:c.1398C>G	XP_011544129.1:p.His466Gln
XM_011545828.1:c.1131C>G	XP_011544130.1:p.His377Gln
XM_011545829.1:c.1101C>G	XP_011544131.1:p.His367Gln
XM_011545830.1:c.1101C>G	XP_011544132.1:p.His367Gln
XM_011545831.1:c.1101C>G	XP_011544133.1:p.His367Gln
XM_011545832.1:c.1101C>G	XP_011544134.1:p.His367Gln
XM_011545833.1:c.1101C>G	XP_011544135.1:p.His367Gln
XM_011545834.1:c.975C>G	XP_011544136.1:p.His325Gln
XM_011545826.2:c.1398C>G	XP_011544128.1:p.His466Gln
XM_011545827.2:c.1398C>G	XP_011544129.1:p.His466Gln
XM_011545828.2:c.1131C>G	XP_011544130.1:p.His377Gln
XM_011545830.2:c.1101C>G	XP_011544132.1:p.His367Gln
XM_011545833.2:c.1101C>G	XP_011544135.1:p.His367Gln
XM_011545834.2:c.975C>G	XP_011544136.1:p.His325Gln
XM_017023211.1:c.*433C>G	XP_016878700.1:n.*433C>G
NM_000418.4:c.1398C>G MANE Select	NP_000409.1:p.His466Gln
NM_001257406.2:c.1398C>G	NP_001244335.1:p.His466Gln
NM_001257407.2:c.1353C>G	NP_001244336.1:p.His451Gln
NM_001257997.2:c.918C>G	NP_001244926.1:p.His306Gln