Canonical Allele Identifier: CA554478147
Gene: IL21 HGNC NCBI

Linked Data

dbSNP Id: rs1294484843

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613806del , CM000666.2:g.122613806del GRCh38
NC_000004.11:g.123534961del , CM000666.1:g.123534961del GRCh37
NC_000004.10:g.123754411del NCBI36
NG_031966.1:g.12254del
NG_031966.2:g.12263del

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.361-876del ENSP00000477555.1:n.361-876del
ENST00000647784.1:n.213-876del
ENST00000648588.1:c.361-876del MANE Select ENSP00000497915.1:n.361-876del
ENST00000264497.7:c.361-876del ENSP00000264497.3:n.361-876del
ENST00000611104.1:c.361-876del ENSP00000477555.1:n.361-876del
NM_001207006.2:c.361-876del NP_001193935.1:n.361-876del
NM_021803.3:c.361-876del NP_068575.1:n.361-876del
NM_021803.4:c.361-876del MANE Select NP_068575.1:n.361-876del
NM_001207006.3:c.361-876del NP_001193935.1:n.361-876del