Canonical Allele Identifier: CA1490366303
Community Standard Title: NM_021803.4(IL21):c.204+1098C=
Gene: IL21 HGNC NCBI
IL21-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122619603G= , CM000666.2:g.122619603G= GRCh38
NC_000004.11:g.123540758G= , CM000666.1:g.123540758G= GRCh37
NC_000004.10:g.123760208G= NCBI36
NG_031966.1:g.6455C=
NG_031966.2:g.6464C=

Transcript Alleles

HGVS Amino-acid Change
NM_021803.4:c.204+1098C= (IL21) MANE Select NP_068575.1:n.204+1098C=
ENST00000648588.1:c.204+1098C= (IL21) MANE Select ENSP00000497915.1:n.204+1098C=
NM_001207006.2:c.204+1098C= (IL21) NP_001193935.1:n.204+1098C=
NM_001207006.3:c.204+1098C= (IL21) NP_001193935.1:n.204+1098C=
NM_021803.3:c.204+1098C= (IL21) NP_068575.1:n.204+1098C=
NR_104126.1:n.510+111G= (IL21-AS1)
ENST00000264497.7:c.204+1098C= (IL21) ENSP00000264497.3:n.204+1098C=
ENST00000611104.1:c.204+1098C= (IL21) ENSP00000477555.1:n.204+1098C=
ENST00000611104.2:c.204+1098C= (IL21) ENSP00000477555.1:n.204+1098C=