Canonical Allele Identifier: CA621692171

Gene: IL21R

Linked Data

• dbSNP Id: rs1303443031
• gnomAD v2: 16-27454269-GT-G
• gnomAD v4: 16-27442948-GT-G
• MyVariant Identifiers: chr16:g.27454270del (hg19) ; chr16:g.27442949del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27442953del , CM000678.2:g.27442953del	GRCh38
NC_000016.9:g.27454274del , CM000678.1:g.27454274del	GRCh37
NC_000016.8:g.27361775del	NCBI36
NG_012222.1:g.45552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.353-14del	ENSP00000513135.1:n.353-14del
ENST00000337929.8:c.353-9del MANE Select	ENSP00000338010.3:n.353-9del
ENST00000337929.7:c.353-9del	ENSP00000338010.3:n.353-9del
ENST00000395754.4:c.353-9del	ENSP00000379103.4:n.353-9del
ENST00000561953.1:n.284del
ENST00000564089.5:c.353-9del	ENSP00000456707.1:n.353-9del
NM_021798.3:c.353-9del	NP_068570.1:n.353-9del
NM_181078.2:c.353-9del	NP_851564.1:n.353-9del
NM_181079.4:c.419-9del	NP_851565.4:n.419-9del
XM_011545857.1:c.419-9del	XP_011544159.1:n.419-9del
XM_011545858.1:c.136-1589del	XP_011544160.1:n.136-1589del
XM_011545857.3:c.419-9del	XP_011544159.1:n.419-9del
XM_011545858.3:c.136-1589del	XP_011544160.1:n.136-1589del
XM_017023257.2:c.353-9del	XP_016878746.1:n.353-9del
NM_181078.3:c.353-9del MANE Select	NP_851564.1:n.353-9del
NM_021798.4:c.353-9del	NP_068570.1:n.353-9del
NM_181079.5:c.419-9del	NP_851565.4:n.419-9del