Canonical Allele Identifier: CA494247183

Gene: IL21R

Linked Data

• MyVariant Identifiers: chr16:g.27454365T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443044T>C , CM000678.2:g.27443044T>C	GRCh38
NC_000016.9:g.27454365T>C , CM000678.1:g.27454365T>C	GRCh37
NC_000016.8:g.27361866T>C	NCBI36
NG_012222.1:g.45643T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*31T>C	ENSP00000513135.1:n.*31T>C
ENST00000337929.8:c.435T>C MANE Select	ENSP00000338010.3:p.Pro145=
ENST00000337929.7:c.435T>C	ENSP00000338010.3:p.Pro145=
ENST00000395754.4:c.435T>C	ENSP00000379103.4:p.Pro145=
ENST00000561953.1:n.375T>C
ENST00000564089.5:c.435T>C	ENSP00000456707.1:p.Pro145=
NM_021798.3:c.435T>C	NP_068570.1:p.Pro145=
NM_181078.2:c.435T>C	NP_851564.1:p.Pro145=
NM_181079.4:c.501T>C	NP_851565.4:p.Pro167=
XM_011545857.1:c.501T>C	XP_011544159.1:p.Pro167=
XM_011545858.1:c.136-1498T>C	XP_011544160.1:n.136-1498T>C
XM_011545857.3:c.501T>C	XP_011544159.1:p.Pro167=
XM_011545858.3:c.136-1498T>C	XP_011544160.1:n.136-1498T>C
XM_017023257.2:c.435T>C	XP_016878746.1:p.Pro145=
NM_181078.3:c.435T>C MANE Select	NP_851564.1:p.Pro145=
NM_021798.4:c.435T>C	NP_068570.1:p.Pro145=
NM_181079.5:c.501T>C	NP_851565.4:p.Pro167=