Canonical Allele Identifier: CA395302038

Gene: IL21R

Linked Data

• dbSNP Id: rs771092403
• gnomAD v2: 16-27454366-G-T
• gnomAD v4: 16-27443045-G-T
• MyVariant Identifiers: chr16:g.27454366G>T (hg19) ; chr16:g.27443045G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443045G>T , CM000678.2:g.27443045G>T	GRCh38
NC_000016.9:g.27454366G>T , CM000678.1:g.27454366G>T	GRCh37
NC_000016.8:g.27361867G>T	NCBI36
NG_012222.1:g.45644G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*32G>T	ENSP00000513135.1:n.*32G>T
ENST00000337929.8:c.436G>T MANE Select	ENSP00000338010.3:p.Ala146Ser
ENST00000337929.7:c.436G>T	ENSP00000338010.3:p.Ala146Ser
ENST00000395754.4:c.436G>T	ENSP00000379103.4:p.Ala146Ser
ENST00000561953.1:n.376G>T
ENST00000564089.5:c.436G>T	ENSP00000456707.1:p.Ala146Ser
NM_021798.3:c.436G>T	NP_068570.1:p.Ala146Ser
NM_181078.2:c.436G>T	NP_851564.1:p.Ala146Ser
NM_181079.4:c.502G>T	NP_851565.4:p.Ala168Ser
XM_011545857.1:c.502G>T	XP_011544159.1:p.Ala168Ser
XM_011545858.1:c.136-1497G>T	XP_011544160.1:n.136-1497G>T
XM_011545857.3:c.502G>T	XP_011544159.1:p.Ala168Ser
XM_011545858.3:c.136-1497G>T	XP_011544160.1:n.136-1497G>T
XM_017023257.2:c.436G>T	XP_016878746.1:p.Ala146Ser
NM_181078.3:c.436G>T MANE Select	NP_851564.1:p.Ala146Ser
NM_021798.4:c.436G>T	NP_068570.1:p.Ala146Ser
NM_181079.5:c.502G>T	NP_851565.4:p.Ala168Ser