Canonical Allele Identifier: CA395302209
Gene: IL21R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27443076A>C , CM000678.2:g.27443076A>C GRCh38
NC_000016.9:g.27454397A>C , CM000678.1:g.27454397A>C GRCh37
NC_000016.8:g.27361898A>C NCBI36
NG_012222.1:g.45675A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697146.1:c.*63A>C ENSP00000513135.1:n.*63A>C
ENST00000337929.8:c.467A>C MANE Select ENSP00000338010.3:p.Tyr156Ser
ENST00000337929.7:c.467A>C ENSP00000338010.3:p.Tyr156Ser
ENST00000395754.4:c.467A>C ENSP00000379103.4:p.Tyr156Ser
ENST00000561953.1:n.407A>C
ENST00000564089.5:c.467A>C ENSP00000456707.1:p.Tyr156Ser
NM_021798.3:c.467A>C NP_068570.1:p.Tyr156Ser
NM_181078.2:c.467A>C NP_851564.1:p.Tyr156Ser
NM_181079.4:c.533A>C NP_851565.4:p.Tyr178Ser
XM_011545857.1:c.533A>C XP_011544159.1:p.Tyr178Ser
XM_011545858.1:c.136-1466A>C XP_011544160.1:n.136-1466A>C
XM_011545857.3:c.533A>C XP_011544159.1:p.Tyr178Ser
XM_011545858.3:c.136-1466A>C XP_011544160.1:n.136-1466A>C
XM_017023257.2:c.467A>C XP_016878746.1:p.Tyr156Ser
NM_181078.3:c.467A>C MANE Select NP_851564.1:p.Tyr156Ser
NM_021798.4:c.467A>C NP_068570.1:p.Tyr156Ser
NM_181079.5:c.533A>C NP_851565.4:p.Tyr178Ser