Canonical Allele Identifier: CA395301860

Gene: IL21R

Linked Data

• MyVariant Identifiers: chr16:g.27454319T>C (hg19) ; chr16:g.27442998T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27442998T>C , CM000678.2:g.27442998T>C	GRCh38
NC_000016.9:g.27454319T>C , CM000678.1:g.27454319T>C	GRCh37
NC_000016.8:g.27361820T>C	NCBI36
NG_012222.1:g.45597T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.384T>C	ENSP00000513135.1:p.Leu128=
ENST00000337929.8:c.389T>C MANE Select	ENSP00000338010.3:p.Phe130Ser
ENST00000337929.7:c.389T>C	ENSP00000338010.3:p.Phe130Ser
ENST00000395754.4:c.389T>C	ENSP00000379103.4:p.Phe130Ser
ENST00000561953.1:n.329T>C
ENST00000564089.5:c.389T>C	ENSP00000456707.1:p.Phe130Ser
NM_021798.3:c.389T>C	NP_068570.1:p.Phe130Ser
NM_181078.2:c.389T>C	NP_851564.1:p.Phe130Ser
NM_181079.4:c.455T>C	NP_851565.4:p.Phe152Ser
XM_011545857.1:c.455T>C	XP_011544159.1:p.Phe152Ser
XM_011545858.1:c.136-1544T>C	XP_011544160.1:n.136-1544T>C
XM_011545857.3:c.455T>C	XP_011544159.1:p.Phe152Ser
XM_011545858.3:c.136-1544T>C	XP_011544160.1:n.136-1544T>C
XM_017023257.2:c.389T>C	XP_016878746.1:p.Phe130Ser
NM_181078.3:c.389T>C MANE Select	NP_851564.1:p.Phe130Ser
NM_021798.4:c.389T>C	NP_068570.1:p.Phe130Ser
NM_181079.5:c.455T>C	NP_851565.4:p.Phe152Ser