Canonical Allele Identifier: CA7974958

Gene: IL21R

Linked Data

• ClinVar Variation Id: 541001
• ClinVar RCV Id: RCV000651180
• dbSNP Id: rs141558701
• ExAC: 16:27454290 G / A
• gnomAD v2: 16-27454290-G-A
• gnomAD v3: 16-27442969-G-A
• gnomAD v4: 16-27442969-G-A
• MyVariant Identifiers: chr16:g.27454290G>A (hg19) ; chr16:g.27442969G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27442969G>A , CM000678.2:g.27442969G>A	GRCh38
NC_000016.9:g.27454290G>A , CM000678.1:g.27454290G>A	GRCh37
NC_000016.8:g.27361791G>A	NCBI36
NG_012222.1:g.45568G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.355G>A	ENSP00000513135.1:p.Gly119Ser
ENST00000337929.8:c.360G>A MANE Select	ENSP00000338010.3:p.Pro120=
ENST00000337929.7:c.360G>A	ENSP00000338010.3:p.Pro120=
ENST00000395754.4:c.360G>A	ENSP00000379103.4:p.Pro120=
ENST00000561953.1:n.300G>A
ENST00000564089.5:c.360G>A	ENSP00000456707.1:p.Pro120=
NM_021798.3:c.360G>A	NP_068570.1:p.Pro120=
NM_181078.2:c.360G>A	NP_851564.1:p.Pro120=
NM_181079.4:c.426G>A	NP_851565.4:p.Pro142=
XM_011545857.1:c.426G>A	XP_011544159.1:p.Pro142=
XM_011545858.1:c.136-1573G>A	XP_011544160.1:n.136-1573G>A
XM_011545857.3:c.426G>A	XP_011544159.1:p.Pro142=
XM_011545858.3:c.136-1573G>A	XP_011544160.1:n.136-1573G>A
XM_017023257.2:c.360G>A	XP_016878746.1:p.Pro120=
NM_181078.3:c.360G>A MANE Select	NP_851564.1:p.Pro120=
NM_021798.4:c.360G>A	NP_068570.1:p.Pro120=
NM_181079.5:c.426G>A	NP_851565.4:p.Pro142=