Canonical Allele Identifier: CA395301853

Gene: IL21R

Linked Data

• ClinVar Variation Id: 843351
• ClinVar RCV Id: RCV001045956
• dbSNP Id: rs2087415911
• MyVariant Identifiers: chr16:g.27454316C>T (hg19) ; chr16:g.27442995C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27442995C>T , CM000678.2:g.27442995C>T	GRCh38
NC_000016.9:g.27454316C>T , CM000678.1:g.27454316C>T	GRCh37
NC_000016.8:g.27361817C>T	NCBI36
NG_012222.1:g.45594C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.381C>T	ENSP00000513135.1:p.Asp127=
ENST00000337929.8:c.386C>T MANE Select	ENSP00000338010.3:p.Thr129Ile
ENST00000337929.7:c.386C>T	ENSP00000338010.3:p.Thr129Ile
ENST00000395754.4:c.386C>T	ENSP00000379103.4:p.Thr129Ile
ENST00000561953.1:n.326C>T
ENST00000564089.5:c.386C>T	ENSP00000456707.1:p.Thr129Ile
NM_021798.3:c.386C>T	NP_068570.1:p.Thr129Ile
NM_181078.2:c.386C>T	NP_851564.1:p.Thr129Ile
NM_181079.4:c.452C>T	NP_851565.4:p.Thr151Ile
XM_011545857.1:c.452C>T	XP_011544159.1:p.Thr151Ile
XM_011545858.1:c.136-1547C>T	XP_011544160.1:n.136-1547C>T
XM_011545857.3:c.452C>T	XP_011544159.1:p.Thr151Ile
XM_011545858.3:c.136-1547C>T	XP_011544160.1:n.136-1547C>T
XM_017023257.2:c.386C>T	XP_016878746.1:p.Thr129Ile
NM_181078.3:c.386C>T MANE Select	NP_851564.1:p.Thr129Ile
NM_021798.4:c.386C>T	NP_068570.1:p.Thr129Ile
NM_181079.5:c.452C>T	NP_851565.4:p.Thr151Ile