Canonical Allele Identifier: CA494247147

Gene: IL21R

Linked Data

• dbSNP Id: rs2141306198
• MyVariant Identifiers: chr16:g.27454308G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27442987G>A , CM000678.2:g.27442987G>A	GRCh38
NC_000016.9:g.27454308G>A , CM000678.1:g.27454308G>A	GRCh37
NC_000016.8:g.27361809G>A	NCBI36
NG_012222.1:g.45586G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.373G>A	ENSP00000513135.1:p.Asp125Asn
ENST00000337929.8:c.378G>A MANE Select	ENSP00000338010.3:p.Val126=
ENST00000337929.7:c.378G>A	ENSP00000338010.3:p.Val126=
ENST00000395754.4:c.378G>A	ENSP00000379103.4:p.Val126=
ENST00000561953.1:n.318G>A
ENST00000564089.5:c.378G>A	ENSP00000456707.1:p.Val126=
NM_021798.3:c.378G>A	NP_068570.1:p.Val126=
NM_181078.2:c.378G>A	NP_851564.1:p.Val126=
NM_181079.4:c.444G>A	NP_851565.4:p.Val148=
XM_011545857.1:c.444G>A	XP_011544159.1:p.Val148=
XM_011545858.1:c.136-1555G>A	XP_011544160.1:n.136-1555G>A
XM_011545857.3:c.444G>A	XP_011544159.1:p.Val148=
XM_011545858.3:c.136-1555G>A	XP_011544160.1:n.136-1555G>A
XM_017023257.2:c.378G>A	XP_016878746.1:p.Val126=
NM_181078.3:c.378G>A MANE Select	NP_851564.1:p.Val126=
NM_021798.4:c.378G>A	NP_068570.1:p.Val126=
NM_181079.5:c.444G>A	NP_851565.4:p.Val148=