Canonical Allele Identifier: CA395302059

Gene: IL21R

Linked Data

• ClinVar Variation Id: 1678067
• ClinVar RCV Id: RCV002224658
• dbSNP Id: rs2141306371
• MyVariant Identifiers: chr16:g.27454371C>G (hg19) ; chr16:g.27443050C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443050C>G , CM000678.2:g.27443050C>G	GRCh38
NC_000016.9:g.27454371C>G , CM000678.1:g.27454371C>G	GRCh37
NC_000016.8:g.27361872C>G	NCBI36
NG_012222.1:g.45649C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*37C>G	ENSP00000513135.1:n.*37C>G
ENST00000337929.8:c.441C>G MANE Select	ENSP00000338010.3:p.Phe147Leu
ENST00000337929.7:c.441C>G	ENSP00000338010.3:p.Phe147Leu
ENST00000395754.4:c.441C>G	ENSP00000379103.4:p.Phe147Leu
ENST00000561953.1:n.381C>G
ENST00000564089.5:c.441C>G	ENSP00000456707.1:p.Phe147Leu
NM_021798.3:c.441C>G	NP_068570.1:p.Phe147Leu
NM_181078.2:c.441C>G	NP_851564.1:p.Phe147Leu
NM_181079.4:c.507C>G	NP_851565.4:p.Phe169Leu
XM_011545857.1:c.507C>G	XP_011544159.1:p.Phe169Leu
XM_011545858.1:c.136-1492C>G	XP_011544160.1:n.136-1492C>G
XM_011545857.3:c.507C>G	XP_011544159.1:p.Phe169Leu
XM_011545858.3:c.136-1492C>G	XP_011544160.1:n.136-1492C>G
XM_017023257.2:c.441C>G	XP_016878746.1:p.Phe147Leu
NM_181078.3:c.441C>G MANE Select	NP_851564.1:p.Phe147Leu
NM_021798.4:c.441C>G	NP_068570.1:p.Phe147Leu
NM_181079.5:c.507C>G	NP_851565.4:p.Phe169Leu