Canonical Allele Identifier: CA2632434529

Gene: IL21R

Linked Data

• gnomAD v4: 16-27442850-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27442850G>T , CM000678.2:g.27442850G>T	GRCh38
NC_000016.9:g.27454171G>T , CM000678.1:g.27454171G>T	GRCh37
NC_000016.8:g.27361672G>T	NCBI36
NG_012222.1:g.45449G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.353-117G>T	ENSP00000513135.1:n.353-117G>T
ENST00000337929.8:c.353-112G>T MANE Select	ENSP00000338010.3:n.353-112G>T
ENST00000337929.7:c.353-112G>T	ENSP00000338010.3:n.353-112G>T
ENST00000395754.4:c.353-112G>T	ENSP00000379103.4:n.353-112G>T
ENST00000561953.1:n.181G>T
ENST00000564089.5:c.353-112G>T	ENSP00000456707.1:n.353-112G>T
NM_021798.3:c.353-112G>T	NP_068570.1:n.353-112G>T
NM_181078.2:c.353-112G>T	NP_851564.1:n.353-112G>T
NM_181079.4:c.419-112G>T	NP_851565.4:n.419-112G>T
XM_011545857.1:c.419-112G>T	XP_011544159.1:n.419-112G>T
XM_011545858.1:c.136-1692G>T	XP_011544160.1:n.136-1692G>T
XM_011545857.3:c.419-112G>T	XP_011544159.1:n.419-112G>T
XM_011545858.3:c.136-1692G>T	XP_011544160.1:n.136-1692G>T
XM_017023257.2:c.353-112G>T	XP_016878746.1:n.353-112G>T
NM_181078.3:c.353-112G>T MANE Select	NP_851564.1:n.353-112G>T
NM_021798.4:c.353-112G>T	NP_068570.1:n.353-112G>T
NM_181079.5:c.419-112G>T	NP_851565.4:n.419-112G>T