Canonical Allele Identifier: CA7975210

Gene: IL21R IL21R-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27449133G>A , CM000678.2:g.27449133G>A	GRCh38
NC_000016.9:g.27460454G>A , CM000678.1:g.27460454G>A	GRCh37
NC_000016.8:g.27367955G>A	NCBI36
NG_012222.1:g.51732G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337929.8:c.1467G>A (IL21R) MANE Select	ENSP00000338010.3:p.Thr489=
ENST00000337929.7:c.1467G>A (IL21R)	ENSP00000338010.3:p.Thr489=
ENST00000395754.4:c.1467G>A (IL21R)	ENSP00000379103.4:p.Thr489=
ENST00000564089.5:c.1467G>A (IL21R)	ENSP00000456707.1:p.Thr489=
NM_021798.3:c.1467G>A (IL21R)	NP_068570.1:p.Thr489=
NM_181078.2:c.1467G>A (IL21R)	NP_851564.1:p.Thr489=
NM_181079.4:c.1533G>A (IL21R)	NP_851565.4:p.Thr511=
NR_037158.1:n.1151C>T (IL21R-AS1)
XM_011545857.1:c.1533G>A (IL21R)	XP_011544159.1:p.Thr511=
XM_011545858.1:c.1095G>A (IL21R)	XP_011544160.1:p.Thr365=
XM_011545857.3:c.1533G>A (IL21R)	XP_011544159.1:p.Thr511=
XM_011545858.3:c.1095G>A (IL21R)	XP_011544160.1:p.Thr365=
XM_017023257.2:c.1467G>A (IL21R)	XP_016878746.1:p.Thr489=
NM_181078.3:c.1467G>A (IL21R) MANE Select	NP_851564.1:p.Thr489=
NM_021798.4:c.1467G>A (IL21R)	NP_068570.1:p.Thr489=
NM_181079.5:c.1533G>A (IL21R)	NP_851565.4:p.Thr511=