Canonical Allele Identifier: CA395301882

Gene: IL21R

Linked Data

• dbSNP Id: rs1196250104
• gnomAD v2: 16-27454325-G-C
• gnomAD v3: 16-27443004-G-C
• gnomAD v4: 16-27443004-G-C
• MyVariant Identifiers: chr16:g.27454325G>C (hg19) ; chr16:g.27443004G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443004G>C , CM000678.2:g.27443004G>C	GRCh38
NC_000016.9:g.27454325G>C , CM000678.1:g.27454325G>C	GRCh37
NC_000016.8:g.27361826G>C	NCBI36
NG_012222.1:g.45603G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.390G>C	ENSP00000513135.1:p.Arg130Ser
ENST00000337929.8:c.395G>C MANE Select	ENSP00000338010.3:p.Gly132Ala
ENST00000337929.7:c.395G>C	ENSP00000338010.3:p.Gly132Ala
ENST00000395754.4:c.395G>C	ENSP00000379103.4:p.Gly132Ala
ENST00000561953.1:n.335G>C
ENST00000564089.5:c.395G>C	ENSP00000456707.1:p.Gly132Ala
NM_021798.3:c.395G>C	NP_068570.1:p.Gly132Ala
NM_181078.2:c.395G>C	NP_851564.1:p.Gly132Ala
NM_181079.4:c.461G>C	NP_851565.4:p.Gly154Ala
XM_011545857.1:c.461G>C	XP_011544159.1:p.Gly154Ala
XM_011545858.1:c.136-1538G>C	XP_011544160.1:n.136-1538G>C
XM_011545857.3:c.461G>C	XP_011544159.1:p.Gly154Ala
XM_011545858.3:c.136-1538G>C	XP_011544160.1:n.136-1538G>C
XM_017023257.2:c.395G>C	XP_016878746.1:p.Gly132Ala
NM_181078.3:c.395G>C MANE Select	NP_851564.1:p.Gly132Ala
NM_021798.4:c.395G>C	NP_068570.1:p.Gly132Ala
NM_181079.5:c.461G>C	NP_851565.4:p.Gly154Ala