Canonical Allele Identifier: CA1490361276

Gene: IL21

Linked Data

• dbSNP Id: rs1799300333

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122613928C>T , CM000666.2:g.122613928C>T	GRCh38
NC_000004.11:g.123535083C>T , CM000666.1:g.123535083C>T	GRCh37
NC_000004.10:g.123754533C>T	NCBI36
NG_031966.1:g.12130G>A
NG_031966.2:g.12139G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000611104.2:c.361-1000G>A	ENSP00000477555.1:n.361-1000G>A
ENST00000647784.1:n.213-1000G>A
ENST00000648588.1:c.361-1000G>A MANE Select	ENSP00000497915.1:n.361-1000G>A
ENST00000264497.7:c.361-1000G>A	ENSP00000264497.3:n.361-1000G>A
ENST00000611104.1:c.361-1000G>A	ENSP00000477555.1:n.361-1000G>A
NM_001207006.2:c.361-1000G>A	NP_001193935.1:n.361-1000G>A
NM_021803.3:c.361-1000G>A	NP_068575.1:n.361-1000G>A
NM_021803.4:c.361-1000G>A MANE Select	NP_068575.1:n.361-1000G>A
NM_001207006.3:c.361-1000G>A	NP_001193935.1:n.361-1000G>A