Canonical Allele Identifier: CA1490361302

Gene: IL21

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122614007A= , CM000666.2:g.122614007A=	GRCh38
NC_000004.11:g.123535162A= , CM000666.1:g.123535162A=	GRCh37
NC_000004.10:g.123754612A=	NCBI36
NG_031966.1:g.12051T=
NG_031966.2:g.12060T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000611104.2:c.361-1079T=	ENSP00000477555.1:n.361-1079T=
ENST00000647784.1:n.213-1079T=
ENST00000648588.1:c.361-1079T= MANE Select	ENSP00000497915.1:n.361-1079T=
ENST00000264497.7:c.361-1079T=	ENSP00000264497.3:n.361-1079T=
ENST00000611104.1:c.361-1079T=	ENSP00000477555.1:n.361-1079T=
NM_001207006.2:c.361-1079T=	NP_001193935.1:n.361-1079T=
NM_021803.3:c.361-1079T=	NP_068575.1:n.361-1079T=
NM_021803.4:c.361-1079T= MANE Select	NP_068575.1:n.361-1079T=
NM_001207006.3:c.361-1079T=	NP_001193935.1:n.361-1079T=