Canonical Allele Identifier: CA494247158

Gene: IL21R

Linked Data

• gnomAD v4: 16-27442996-C-T
• MyVariant Identifiers: chr16:g.27454317C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27442996C>T , CM000678.2:g.27442996C>T	GRCh38
NC_000016.9:g.27454317C>T , CM000678.1:g.27454317C>T	GRCh37
NC_000016.8:g.27361818C>T	NCBI36
NG_012222.1:g.45595C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.382C>T	ENSP00000513135.1:p.Leu128Phe
ENST00000337929.8:c.387C>T MANE Select	ENSP00000338010.3:p.Thr129=
ENST00000337929.7:c.387C>T	ENSP00000338010.3:p.Thr129=
ENST00000395754.4:c.387C>T	ENSP00000379103.4:p.Thr129=
ENST00000561953.1:n.327C>T
ENST00000564089.5:c.387C>T	ENSP00000456707.1:p.Thr129=
NM_021798.3:c.387C>T	NP_068570.1:p.Thr129=
NM_181078.2:c.387C>T	NP_851564.1:p.Thr129=
NM_181079.4:c.453C>T	NP_851565.4:p.Thr151=
XM_011545857.1:c.453C>T	XP_011544159.1:p.Thr151=
XM_011545858.1:c.136-1546C>T	XP_011544160.1:n.136-1546C>T
XM_011545857.3:c.453C>T	XP_011544159.1:p.Thr151=
XM_011545858.3:c.136-1546C>T	XP_011544160.1:n.136-1546C>T
XM_017023257.2:c.387C>T	XP_016878746.1:p.Thr129=
NM_181078.3:c.387C>T MANE Select	NP_851564.1:p.Thr129=
NM_021798.4:c.387C>T	NP_068570.1:p.Thr129=
NM_181079.5:c.453C>T	NP_851565.4:p.Thr151=