Canonical Allele Identifier: CA14244719

Gene: IL21R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27423717C>A , CM000678.2:g.27423717C>A	GRCh38
NC_000016.9:g.27435038C>A , CM000678.1:g.27435038C>A	GRCh37
NC_000016.8:g.27342539C>A	NCBI36
NG_012222.1:g.26316C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337929.8:c.-16-6339C>A MANE Select	ENSP00000338010.3:n.-16-6339C>A
ENST00000337929.7:c.-16-6339C>A	ENSP00000338010.3:n.-16-6339C>A
ENST00000564089.5:c.-16-6339C>A	ENSP00000456707.1:n.-16-6339C>A
NM_181078.2:c.-16-6339C>A	NP_851564.1:n.-16-6339C>A
NM_181079.4:c.51-6339C>A	NP_851565.4:n.51-6339C>A
XM_011545857.1:c.51-6339C>A	XP_011544159.1:n.51-6339C>A
XM_011545858.1:c.-233-6339C>A	XP_011544160.1:n.-233-6339C>A
XM_011545857.3:c.51-6339C>A	XP_011544159.1:n.51-6339C>A
XM_011545858.3:c.-233-6339C>A	XP_011544160.1:n.-233-6339C>A
XM_017023257.2:c.-16-6339C>A	XP_016878746.1:n.-16-6339C>A
NM_181078.3:c.-16-6339C>A MANE Select	NP_851564.1:n.-16-6339C>A
NM_181079.5:c.51-6339C>A	NP_851565.4:n.51-6339C>A