Canonical Allele Identifier: CA105236325

Gene: IL21 IL21-AS1

Linked Data

• dbSNP Id: rs80293267
• MyVariant Identifiers: chr4:g.123540675T>A (hg19) ; chr4:g.122619520T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122619520T>A , CM000666.2:g.122619520T>A	GRCh38
NC_000004.11:g.123540675T>A , CM000666.1:g.123540675T>A	GRCh37
NC_000004.10:g.123760125T>A	NCBI36
NG_031966.1:g.6538A>T
NG_031966.2:g.6547A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000611104.2:c.204+1181A>T (IL21)	ENSP00000477555.1:n.204+1181A>T
ENST00000648588.1:c.204+1181A>T (IL21) MANE Select	ENSP00000497915.1:n.204+1181A>T
ENST00000264497.7:c.204+1181A>T (IL21)	ENSP00000264497.3:n.204+1181A>T
ENST00000611104.1:c.204+1181A>T (IL21)	ENSP00000477555.1:n.204+1181A>T
NM_001207006.2:c.204+1181A>T (IL21)	NP_001193935.1:n.204+1181A>T
NM_021803.3:c.204+1181A>T (IL21)	NP_068575.1:n.204+1181A>T
NR_104126.1:n.510+28T>A (IL21-AS1)
NM_021803.4:c.204+1181A>T (IL21) MANE Select	NP_068575.1:n.204+1181A>T
NM_001207006.3:c.204+1181A>T (IL21)	NP_001193935.1:n.204+1181A>T