Canonical Allele Identifier: CA395302412

Gene: IL21R

Linked Data

• MyVariant Identifiers: chr16:g.27454432G>C (hg19) ; chr16:g.27443111G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443111G>C , CM000678.2:g.27443111G>C	GRCh38
NC_000016.9:g.27454432G>C , CM000678.1:g.27454432G>C	GRCh37
NC_000016.8:g.27361933G>C	NCBI36
NG_012222.1:g.45710G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*98G>C	ENSP00000513135.1:n.*98G>C
ENST00000337929.8:c.502G>C MANE Select	ENSP00000338010.3:p.Ala168Pro
ENST00000337929.7:c.502G>C	ENSP00000338010.3:p.Ala168Pro
ENST00000395754.4:c.502G>C	ENSP00000379103.4:p.Ala168Pro
ENST00000561953.1:n.442G>C
ENST00000564089.5:c.502G>C	ENSP00000456707.1:p.Ala168Pro
NM_021798.3:c.502G>C	NP_068570.1:p.Ala168Pro
NM_181078.2:c.502G>C	NP_851564.1:p.Ala168Pro
NM_181079.4:c.568G>C	NP_851565.4:p.Ala190Pro
XM_011545857.1:c.568G>C	XP_011544159.1:p.Ala190Pro
XM_011545858.1:c.136-1431G>C	XP_011544160.1:n.136-1431G>C
XM_011545857.3:c.568G>C	XP_011544159.1:p.Ala190Pro
XM_011545858.3:c.136-1431G>C	XP_011544160.1:n.136-1431G>C
XM_017023257.2:c.502G>C	XP_016878746.1:p.Ala168Pro
NM_181078.3:c.502G>C MANE Select	NP_851564.1:p.Ala168Pro
NM_021798.4:c.502G>C	NP_068570.1:p.Ala168Pro
NM_181079.5:c.568G>C	NP_851565.4:p.Ala190Pro