Canonical Allele Identifier: CA7974800

Gene: IL21R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27403181G>A , CM000678.2:g.27403181G>A	GRCh38
NC_000016.9:g.27414502G>A , CM000678.1:g.27414502G>A	GRCh37
NC_000016.8:g.27322003G>A	NCBI36
NG_012222.1:g.5780G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337929.8:c.-17+563G>A MANE Select	ENSP00000338010.3:n.-17+563G>A
ENST00000337929.7:c.-17+563G>A	ENSP00000338010.3:n.-17+563G>A
ENST00000564089.5:c.-56G>A	ENSP00000456707.1:n.-56G>A
NM_181078.2:c.-17+563G>A	NP_851564.1:n.-17+563G>A
NM_181079.4:c.11G>A	NP_851565.4:p.Arg4His
XM_011545857.1:c.11G>A	XP_011544159.1:p.Arg4His
XM_011545858.1:c.-273G>A	XP_011544160.1:n.-273G>A
XM_011545857.3:c.11G>A	XP_011544159.1:p.Arg4His
XM_011545858.3:c.-273G>A	XP_011544160.1:n.-273G>A
XM_017023257.2:c.-147+563G>A	XP_016878746.1:n.-147+563G>A
NM_181078.3:c.-17+563G>A MANE Select	NP_851564.1:n.-17+563G>A
NM_181079.5:c.11G>A	NP_851565.4:p.Arg4His