Canonical Allele Identifier: CA1490366335
Gene: IL21 HGNC NCBI
IL21-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122619688C= , CM000666.2:g.122619688C= GRCh38
NC_000004.11:g.123540843C= , CM000666.1:g.123540843C= GRCh37
NC_000004.10:g.123760293C= NCBI36
NG_031966.1:g.6370G=
NG_031966.2:g.6379G=

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.204+1013G= (IL21) ENSP00000477555.1:n.204+1013G=
ENST00000648588.1:c.204+1013G= (IL21) MANE Select ENSP00000497915.1:n.204+1013G=
ENST00000264497.7:c.204+1013G= (IL21) ENSP00000264497.3:n.204+1013G=
ENST00000611104.1:c.204+1013G= (IL21) ENSP00000477555.1:n.204+1013G=
NM_001207006.2:c.204+1013G= (IL21) NP_001193935.1:n.204+1013G=
NM_021803.3:c.204+1013G= (IL21) NP_068575.1:n.204+1013G=
NR_104126.1:n.510+196C= (IL21-AS1)
NM_021803.4:c.204+1013G= (IL21) MANE Select NP_068575.1:n.204+1013G=
NM_001207006.3:c.204+1013G= (IL21) NP_001193935.1:n.204+1013G=
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