Canonical Allele Identifier: CA7974960

Gene: IL21R

Linked Data

• dbSNP Id: rs763781299
• ExAC: 16:27454299 T / G
• gnomAD v2: 16-27454299-T-G
• MyVariant Identifiers: chr16:g.27454299T>G (hg19) ; chr16:g.27442978T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27442978T>G , CM000678.2:g.27442978T>G	GRCh38
NC_000016.9:g.27454299T>G , CM000678.1:g.27454299T>G	GRCh37
NC_000016.8:g.27361800T>G	NCBI36
NG_012222.1:g.45577T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.364T>G	ENSP00000513135.1:p.Phe122Val
ENST00000337929.8:c.369T>G MANE Select	ENSP00000338010.3:p.Pro123=
ENST00000337929.7:c.369T>G	ENSP00000338010.3:p.Pro123=
ENST00000395754.4:c.369T>G	ENSP00000379103.4:p.Pro123=
ENST00000561953.1:n.309T>G
ENST00000564089.5:c.369T>G	ENSP00000456707.1:p.Pro123=
NM_021798.3:c.369T>G	NP_068570.1:p.Pro123=
NM_181078.2:c.369T>G	NP_851564.1:p.Pro123=
NM_181079.4:c.435T>G	NP_851565.4:p.Pro145=
XM_011545857.1:c.435T>G	XP_011544159.1:p.Pro145=
XM_011545858.1:c.136-1564T>G	XP_011544160.1:n.136-1564T>G
XM_011545857.3:c.435T>G	XP_011544159.1:p.Pro145=
XM_011545858.3:c.136-1564T>G	XP_011544160.1:n.136-1564T>G
XM_017023257.2:c.369T>G	XP_016878746.1:p.Pro123=
NM_181078.3:c.369T>G MANE Select	NP_851564.1:p.Pro123=
NM_021798.4:c.369T>G	NP_068570.1:p.Pro123=
NM_181079.5:c.435T>G	NP_851565.4:p.Pro145=